What is NDC 68788-7774?

68788-7774 is the product NDC for Gabapentin, Gabapentin 800 mg/1 tablet, listed with the FDA by Preferred Pharmaceuticals, Inc.. It has 5 package NDCs, shown above in 10- and 11-digit form.

Preferred Pharmaceuticals, Inc., NDC labeler code 68788. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Gabapentin?

561 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Gabapentin NDC 68788-7774 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)68788-7774Labeler and product segments. Claims need a package NDC.

Product NDC at billing width68788-7774Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package
68788-7774-1	68788777401	100 TABLET in 1 BOTTLE (68788-7774-1)Marketed from Aug 24, 2020
68788-7774-3	68788777403	30 TABLET in 1 BOTTLE (68788-7774-3)Marketed from Aug 24, 2020
68788-7774-6	68788777406	60 TABLET in 1 BOTTLE (68788-7774-6)Marketed from Aug 24, 2020
68788-7774-8	68788777408	120 TABLET in 1 BOTTLE (68788-7774-8)Marketed from Aug 24, 2020
68788-7774-9	68788777409	90 TABLET in 1 BOTTLE (68788-7774-9)Marketed from Aug 24, 2020

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary): Gabapentin
Generic name (nonproprietary): gabapentin
Active ingredients: Gabapentin — 800 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Preferred Pharmaceuticals, Inc.NDC labeler code 68788
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 205101
Marketing start: Aug 24, 2020
Listing expires: Dec 31, 2026
Other FDA classes: Decreased Central Nervous System Disorganized Electrical Activity (Physiologic effect)
Identifiers: Product ID 68788-7774_9a21dd1d-c795-4e56-b930-55dbb9254b71SPL ID 9a21dd1d-c795-4e56-b930-55dbb9254b71SPL set ID 5d3f27bf-3486-40fa-a4d3-5f0b2c6c0151RxCUI 310434UNII 6CW7F3G59X

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N468788777401 followed by a unit qualifier and the quantity

Package 68788-7774-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective Jun 11, 2025.

Indications (excerpt from the label)

Gabapentin is indicated for: • Management of postherpetic neuralgia in adults • Adjunctive therapy in the treatment of partial onset seizures, with and without secondary generalization, in adults and pediatric patients 3 years and older with epilepsy Gabapentin is indicated for: • Postherpetic neuralgia in adults ( 1 ) • Adjunctive therapy in the treatment of partial onset seizures, with and without secondary generalization, in adults and pediatric patients 3 years and older with epilepsy ( 1 )

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 68788-7774

What is NDC 68788-7774?: 68788-7774 is the product NDC for Gabapentin, Gabapentin 800 mg/1 tablet, listed with the FDA by Preferred Pharmaceuticals, Inc.. It has 5 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Gabapentin.
What is the active ingredient?: Gabapentin.
Who is the labeler?: Preferred Pharmaceuticals, Inc., NDC labeler code 68788. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Gabapentin?: 561 other product NDCs are listed under this name. See all Gabapentin NDCs.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Gabapentin NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
gabapentin	Gabapentin 300 mg/1	CapsuleOral	REMEDYREPACK INC.	70518-4763	70518-4763-00
Gabapentin	Gabapentin 100 mg/1	CapsuleOral	Advanced Rx of Tennessee, LLC	80425-0595	80425-0595-0180425-0595-0280425-0595-03+1 more
Gabapentin	Gabapentin 100 mg/1	CapsuleOral	Cardinal Health 107, LLC	55154-0581	55154-0581-00
Gabapentin	Gabapentin 300 mg/1	CapsuleOral	REMEDYREPACK INC.	70518-4746	70518-4746-0070518-4746-0170518-4746-02
Gabapentin	Gabapentin 100 mg/1	CapsuleOral	REMEDYREPACK INC.	70518-4742	70518-4742-00
Gabapentin	Gabapentin 400 mg/1	CapsuleOral	REMEDYREPACK INC.	70518-4740	70518-4740-00
Gabapentin	Gabapentin 300 mg/1	CapsuleOral	Cardinal Health 107, LLC	55154-0580	55154-0580-00
Gabapentin	Gabapentin 600 mg/1	Tablet, CoatedOral	Coupler LLC	67046-1233	67046-1233-03
Gabapentin	Gabapentin 200 mg/1	CapsuleOral	Trifluent Pharma, LLC	73352-231	73352-0231-01
Gabapentin	Gabapentin 600 mg/1	TabletOral	Coupler LLC	67046-1086	67046-1086-03

All 562 Gabapentin NDCs

Other NDCs under ANDA 205101

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under ANDA 205101
Product	Strength	Form · route	Labeler	Product NDC
Gabapentin	Gabapentin 800 mg/1	TabletOral	Asclemed USA, Inc.	76420-497
Gabapentin	Gabapentin 600 mg/1	TabletOral	Proficient Rx LP	82804-015
Gabapentin	Gabapentin 800 mg/1	TabletOral	DIRECT RX	72189-178
Gabapentin	Gabapentin 600 mg/1	TabletOral	Bryant Ranch Prepack	72162-1530
Gabapentin	Gabapentin 600 mg/1	TabletOral	HAWAII REPACK, INC.	85534-0009
Gabapentin	Gabapentin 800 mg/1	TabletOral	HAWAII REPACK, INC.	85534-0010
Gabapentin	Gabapentin 800 mg/1	TabletOral	Bryant Ranch Prepack	72162-1531
Gabapentin	Gabapentin 800 mg/1	TabletOral	Preferred Pharmaceuticals, Inc.	68788-7757
Gabapentin	Gabapentin 600 mg/1	TabletOral	Radha Pharmaceuticals, Inc.	77771-177
Gabapentin	Gabapentin 800 mg/1	TabletOral	Radha Pharmaceuticals, Inc.	77771-178
Gabapentin	Gabapentin 600 mg/1	TabletOral	Creekwood Pharmaceuticals LLC	82619-145
Gabapentin	Gabapentin 800 mg/1	TabletOral	Creekwood Pharmaceuticals LLC	82619-146
Gabapentin	Gabapentin 800 mg/1	TabletOral	Proficient Rx LP	71205-774
Gabapentin	Gabapentin 800 mg/1	TabletOral	Proficient Rx LP	71205-514
Gabapentin	Gabapentin 600 mg/1	TabletOral	Directrx	72189-313
Gabapentin	Gabapentin 600 mg/1	TabletOral	Asclemed USA, Inc.	76420-235
Gabapentin	Gabapentin 600 mg/1	TabletOral	Proficient Rx LP	71205-533
Gabapentin	Gabapentin 800 mg/1	TabletOral	PD-Rx Pharmaceuticals, Inc.	72789-217
Gabapentin	Gabapentin 800 mg/1	TabletOral	St. Mary's Medical Park Pharmacy	60760-517
Gabapentin	Gabapentin 800 mg/1	TabletOral	Aphena Pharma Solutions - Tennessee, LLC	71610-737

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