What is NDC 80425-0201?

80425-0201 is the product NDC for Gabapentin, Gabapentin 600 mg/1 tablet, coated, listed with the FDA by Advanced Rx of Tennessee, LLC. It has 4 package NDCs, shown above in 10- and 11-digit form.

Advanced Rx of Tennessee, LLC, NDC labeler code 80425. 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 80425-0201 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)80425-0201Labeler and product segments. Claims need a package NDC.

Product NDC at billing width80425-0201Add 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
80425-0201-1	8042502010180425020101	30 TABLET, COATED in 1 BOTTLE (80425-0201-1)Marketed from Oct 28, 2022
80425-0201-2	8042502010280425020102	60 TABLET, COATED in 1 BOTTLE (80425-0201-2)Marketed from Oct 28, 2022
80425-0201-3	8042502010380425020103	90 TABLET, COATED in 1 BOTTLE (80425-0201-3)Marketed from Oct 28, 2022
80425-0201-4	8042502010480425020104	120 TABLET, COATED in 1 BOTTLE (80425-0201-4)Marketed from Oct 28, 2022

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 — 600 mg/1
Dosage form: Tablet, Coated
Route: Oral
Labeler: Advanced Rx of Tennessee, LLCNDC labeler code 80425
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 207057
Marketing start: Oct 28, 2022
Listing expires: Dec 31, 2026
Other FDA classes: Decreased Central Nervous System Disorganized Electrical Activity (Physiologic effect)
Identifiers: Product ID 80425-0201_2a99e9e8-3d19-ee0b-e063-6294a90ae4efSPL ID 2a99e9e8-3d19-ee0b-e063-6294a90ae4efSPL set ID ec1a01fe-5531-21df-e053-2a95a90a0561RxCUI 310433, 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

N480425020101 followed by a unit qualifier and the quantity

Package 80425-0201-01. 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 Dec 31, 2024.

Indications (excerpt from the label)

1. Indications and Usage 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

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 80425-0201

What is NDC 80425-0201?: 80425-0201 is the product NDC for Gabapentin, Gabapentin 600 mg/1 tablet, coated, listed with the FDA by Advanced Rx of Tennessee, LLC. It has 4 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?: Advanced Rx of Tennessee, LLC, NDC labeler code 80425. 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 800 mg/1	TabletOral	St. Mary's Medical Park Pharmacy	60760-943	60760-0943-3060760-0943-90
gabapentin	Gabapentin 300 mg/1	CapsuleOral	REMEDYREPACK INC.	70518-4763	70518-4763-00
Gabapentin	Gabapentin 100 mg/1	CapsuleOral	Cardinal Health 107, LLC	55154-0581	55154-0581-00
Gabapentin	Gabapentin 100 mg/1	CapsuleOral	Advanced Rx of Tennessee, LLC	80425-0595	80425-0595-0180425-0595-0280425-0595-03+1 more
Gabapentin	Gabapentin 300 mg/1	CapsuleOral	REMEDYREPACK INC.	70518-4746	70518-4746-0070518-4746-0170518-4746-02+1 more
Gabapentin	Gabapentin 100 mg/1	CapsuleOral	REMEDYREPACK INC.	70518-4742	70518-4742-0070518-4742-02
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

All 562 Gabapentin NDCs

Other NDCs under ANDA 207057

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

FDA NDC Directory listings under ANDA 207057
Product	Strength	Form · route	Labeler	Product NDC
Gabapentin	Gabapentin 600 mg/1	Tablet, CoatedOral	TAGI Pharma, Inc.	51224-021
Gabapentin	Gabapentin 600 mg/1	Tablet, CoatedOral	A-S Medication Solutions	50090-7268
Gabapentin	Gabapentin 600 mg/1	Tablet, CoatedOral	A-S Medication Solutions	50090-7269
Gabapentin	Gabapentin 800 mg/1	Tablet, CoatedOral	TAGI Pharma, Inc.	51224-121
Gabapentin	Gabapentin 600 mg/1	Tablet, CoatedOral	Mullan Pharmaceutical Inc.	83301-0001
Gabapentin	Gabapentin 800 mg/1	Tablet, CoatedOral	Mullan Pharmaceutical Inc.	83301-0002
Gabapentin	Gabapentin 800 mg/1	Tablet, CoatedOral	NuCare Pharmaceuticals,Inc.	68071-3523
Gabapentin	Gabapentin 800 mg/1	Tablet, CoatedOral	Proficient Rx LP	82804-203
Gabapentin	Gabapentin 600 mg/1	Tablet, CoatedOral	NuCare Pharmaceuticals, Inc.	68071-3783
Gabapentin	Gabapentin 600 mg/1	Tablet, CoatedOral	Proficient Rx LP	82804-210
Gabapentin	Gabapentin 600 mg/1	Tablet, CoatedOral	Coupler LLC	67046-1233
Gabapentin	Gabapentin 600 mg/1	Tablet, CoatedOral	Precision Dose, Inc.	68094-069
Gabapentin	Gabapentin 800 mg/1	Tablet, CoatedOral	Westminster Pharmaceuticals, LLC	69367-347
Gabapentin	Gabapentin 600 mg/1	Tablet, CoatedOral	Westminster Pharmaceuticals, LLC	69367-346
Gabapentin	Gabapentin 600 mg/1	Tablet, CoatedOral	AvPAK	50268-325
Gabapentin	Gabapentin 800 mg/1	Tablet, CoatedOral	Precision Dose, Inc.	68094-489
Gabapentin	Gabapentin 800 mg/1	Tablet, CoatedOral	A-S Medication Solutions	50090-7400
Gabapentin	Gabapentin 600 mg/1	Tablet, CoatedOral	Precision Dose, Inc.	68094-589
Gabapentin	Gabapentin 600 mg/1	Tablet, CoatedOral	Bryant Ranch Prepack	71335-1287
Gabapentin	Gabapentin 800 mg/1	Tablet, CoatedOral	Advanced Rx of Tennessee, LLC	80425-0204