Good fit
- Qualified oil-based or suspension formulations
- Production requiring automatic capsule separation and liquid dosing
- Hard gelatin or HPMC capsules approved for the formulation
- Projects with defined fill, closing and sealing acceptance tests
NJP-260L · liquid-filled hard capsules
Configure a production-scale liquid capsule filler around formulation compatibility, dose window, capsule shell, sealing route, utilities and acceptance evidence.
Project boundary
A liquid capsule filling machine separates hard-capsule bodies and caps, meters a defined liquid or suspension into the capsule body, closes the capsule and discharges it for the next process. It is not a universal route for every liquid. Shell material, water activity, solvent system, viscosity, temperature, suspended solids and fill level must be reviewed together.
The NJP-260L is intended for defined liquid-filled hard capsule projects using hard gelatin or HPMC shells within an approved formulation window. Oils, qualified suspensions and temperature-managed semi-solid systems may be evaluated. A representative product trial should establish pump settings, dose repeatability, capsule integrity, cleaning method and the need for downstream band sealing.
Operating sequence
Empty capsules are oriented, loaded into mould segments and separated into caps and bodies.
The formulation is held within its qualified mixing, temperature and viscosity window before dosing.
The liquid dosing system delivers the approved volume into each present capsule body.
Capsules are closed and discharged for inspection and, when required, downstream band sealing.




Use representative capsule shells and enough formulation to reach stable operation. Record start-up rejects, fill-weight samples, capsule deformation, leakage observations, pump repeatability and cleaning recovery. A short demonstration without an agreed sampling plan cannot establish sustained output.
Verified technical window
| Parameter | Published specification | Buyer verification |
|---|---|---|
| Rated output | Up to 260 capsules/minute; 15,600 capsules/hour | Confirm sustained good output with representative liquid and capsules. |
| Capsule range | 00#, 0#, 1#, 2#, 3#, 4#, 5# and safety capsules A–E | List every required tooling set and shell supplier in the quotation. |
| Capsule loading rate | ≥99.5% under stated conditions | Agree sample size, run duration and defect definition. |
| Liquid fill variation | ≤±3% for doses of 300 mg or more | Other doses and formulations require project evaluation and trial evidence. |
| Optional dosing routes | Pellet dosing and small-capsule device listed as options | Define sequence, dose split and acceptance method for combination fills. |
| Published controls | Servo-driven PLC/HMI configuration | Confirm final controller, HMI, drive models and substitution control in the approved quotation. |
| Product-contact material | SS316L; non-contact exterior parts SS304 | Request the material records required by the quality team. |
| Overall dimensions | 1020 × 860 × 1970 mm | Add loading, cleaning, service and sealing-line clearances. |
| Machine weight | 900 kg | Confirm floor loading and the receiving/access route. |
| Total motor power | 5.75 kW | Confirm the final connected load and destination electrical standard. |
| Noise | ≤75 dBA | Define measurement position and operating condition if used for acceptance. |
Published figures are configuration-dependent. The approved technical agreement and representative-product FAT control the final project scope.
Need a formulation and capacity review?
Send the capsule, liquid properties, target dose and required good output before comparing quotations.
Filling versus sealing
The NJP-260L fills and closes hard capsules. Depending on the formulation, capsule shell and leakage-risk assessment, the project may also require a separate capsule band-sealing step. Do not assume that mechanical capsule closing creates the same barrier as a qualified band seal.

Capacity planning
Good capsules per shift = verified stable rate × scheduled run time × agreed operating factor.
Do not calculate yearly output from the published maximum alone. Include material conditioning, line clearance, cleaning, sample checks, rejects and the actual downstream constraint.
Controls and utilities
| Utility / condition | Published requirement |
|---|---|
| Power | 3-phase, 4-wire AC 380 V, 50 Hz |
| Vacuum | −0.02 to −0.06 MPa |
| Compressed air | 0.06 m³/min at 0.3 MPa |
| Water flow | 250 L/hour; inlet 20 mm; drain 27 mm |
| Air displacement | 300 m³/hour |
| Room temperature | 21 ±3 °C |
| Relative humidity | 40–55% |
| Ceiling height | ≥2.6 m manual feed; ≥2.8 m vacuum feed |
Define the liquid-tank heating and mixing functions, capsule presence detection, recipe fields, alarm history, user levels, external interlocks and safe recovery after a stop. If a band sealer or inspection device is included, document every handshake signal and reject responsibility.

Quotation scope

A public price without the formulation, capsule, tooling, sealing and documentation scope is not a reliable project budget. Ask each supplier to quote against the same URS and acceptance method.
Make the quotation comparable.
HIJ can separate the machine, tooling, liquid handling, sealing, documents and delivery scope.
URS and FAT inputs
The most useful FAT result is not “machine ran successfully.” It is a traceable data set: formulation condition, capsule lot, run duration, good output, weight samples, rejects, leakage observations and cleaning evidence.
Use the capsule filling machine FAT checklist and GMP validation guide to align engineering and quality teams.



Equipment route
For qualified liquids, oils, suspensions and defined combination-fill projects using hard capsules.
Compare capsule filling routesFor production-scale powders, granules and pellets that do not require liquid handling.
Review the automatic NJP platformFor smaller powder or granule batches where manual plate transfer remains acceptable.
Compare the semi-automatic routeIf unit-dose packaging follows filling and sealing, review the capsule blister packing machine. For model selection, use the capsule filling machine size-selection guide. Service boundaries are explained on the service and support page.
Engineering resources
Buyer questions
It is intended for qualified liquid-filled hard capsule projects, including defined oils, suspensions and temperature-managed semi-solid formulations. Final suitability depends on formulation properties, capsule-shell compatibility, dosing trials, cleaning requirements and the approved project configuration.
The documented rated output is up to 260 capsules per minute, or 15,600 capsules per hour. Sustained good output depends on the formulation, working temperature, capsule, dose, inspection method and downstream sealing or packaging constraint.
The published range is standard hard capsule sizes 00# through 5#, plus safety capsules A–E. Confirm every required shell, supplier and dedicated tooling set during the configuration review.
The published technical value is no more than plus or minus 3% for doses of 300 mg or more. Other dose levels, viscosities and suspension systems require project-specific evaluation and an agreed trial method.
The NJP-260L fills and mechanically closes hard capsules. Some formulations also require a separate capsule band-sealing process. The need for band sealing must be decided from shell compatibility, fill level, formulation behaviour and an agreed leakage challenge.
The published configuration lists 3-phase 380 V at 50 Hz, vacuum from −0.02 to −0.06 MPa, compressed air of 0.06 m³/min at 0.3 MPa, water flow of 250 L/hour, air displacement of 300 m³/hour, room temperature of 21 ±3 °C and relative humidity of 40–55%. Confirm final connection points and destination standards in the approved drawings.
Provide capsule samples, shell information, liquid composition, viscosity and temperature data, target dose and variation, required good output, batch and cleaning plan, sealing and inspection requirements, utilities, control interfaces and the documentation and acceptance evidence required by your quality team.
Specifications and performance statements remain subject to the approved formulation, machine configuration, technical agreement and representative-product testing.
Send formulation properties, capsule samples, target dose, required good output, facility utilities, sealing requirements and FAT scope. HIJ will review the project boundary and return an itemized configuration.
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