NDC codes

FDA NDC Directory
Product NDC (as listed)71335-1287Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71335-1287Add 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 NDC11-digit (billing)PackageCopy
71335-1287-07133512870028 TABLET, COATED in 1 BOTTLE (71335-1287-0)Marketed from Dec 28, 2021
71335-1287-17133512870130 TABLET, COATED in 1 BOTTLE (71335-1287-1)Marketed from Dec 28, 2021
71335-1287-27133512870260 TABLET, COATED in 1 BOTTLE (71335-1287-2)Marketed from Aug 21, 2019
71335-1287-371335128703180 TABLET, COATED in 1 BOTTLE (71335-1287-3)Marketed from Dec 28, 2021
71335-1287-47133512870490 TABLET, COATED in 1 BOTTLE (71335-1287-4)Marketed from Aug 28, 2019
71335-1287-571335128705100 TABLET, COATED in 1 BOTTLE (71335-1287-5)Marketed from Dec 28, 2021
71335-1287-671335128706120 TABLET, COATED in 1 BOTTLE (71335-1287-6)Marketed from Aug 27, 2019
71335-1287-771335128707500 TABLET, COATED in 1 BOTTLE (71335-1287-7)Marketed from Dec 28, 2021
71335-1287-87133512870884 TABLET, COATED in 1 BOTTLE (71335-1287-8)Marketed from Dec 28, 2021
71335-1287-971335128709112 TABLET, COATED in 1 BOTTLE (71335-1287-9)Marketed from Dec 28, 2021

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
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 207057
Marketing start
Listing expires
Other FDA classes
Decreased Central Nervous System Disorganized Electrical Activity (Physiologic effect)
Identifiers
Product ID 71335-1287_1d171bd2-0093-4327-9111-e883bd241e8cSPL ID 1d171bd2-0093-4327-9111-e883bd241e8cSPL set ID d8604417-9d43-4d27-a7ce-d4120ff201f4RxCUI 310433UNII 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

N471335128700 followed by a unit qualifier and the quantity

Package 71335-1287-00. 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 .

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)

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
ProductStrengthForm · routeLabelerProduct NDC
GabapentinGabapentin 800 mg/1Tablet, CoatedOralWestminster Pharmaceuticals, LLC69367-347
GabapentinGabapentin 600 mg/1Tablet, CoatedOralWestminster Pharmaceuticals, LLC69367-346
GabapentinGabapentin 800 mg/1Tablet, CoatedOralMullan Pharmaceutical Inc.83301-0002
GabapentinGabapentin 600 mg/1Tablet, CoatedOralMullan Pharmaceutical Inc.83301-0001
GabapentinGabapentin 600 mg/1Tablet, CoatedOralAdvanced Rx of Tennessee, LLC80425-0201
GabapentinGabapentin 800 mg/1Tablet, CoatedOralAdvanced Rx of Tennessee, LLC80425-0204
GabapentinGabapentin 800 mg/1Tablet, CoatedOralA-S Medication Solutions50090-7400
GabapentinGabapentin 800 mg/1Tablet, CoatedOralProficient Rx LP82804-203
GabapentinGabapentin 600 mg/1Tablet, CoatedOralProficient Rx LP82804-210
GabapentinGabapentin 600 mg/1Tablet, CoatedOralTAGI Pharma, Inc.51224-021
GabapentinGabapentin 800 mg/1Tablet, CoatedOralTAGI Pharma, Inc.51224-121
GabapentinGabapentin 800 mg/1Tablet, CoatedOralNuCare Pharmaceuticals,Inc.68071-3523
GabapentinGabapentin 600 mg/1Tablet, CoatedOralA-S Medication Solutions50090-7268
GabapentinGabapentin 600 mg/1Tablet, CoatedOralPrecision Dose, Inc.68094-069
GabapentinGabapentin 600 mg/1Tablet, CoatedOralNuCare Pharmaceuticals, Inc.68071-3783
GabapentinGabapentin 600 mg/1Tablet, CoatedOralA-S Medication Solutions50090-7269
GabapentinGabapentin 600 mg/1Tablet, CoatedOralCoupler LLC67046-1233
GabapentinGabapentin 800 mg/1Tablet, CoatedOralPrecision Dose, Inc.68094-489
GabapentinGabapentin 600 mg/1Tablet, CoatedOralAvPAK50268-325
GabapentinGabapentin 600 mg/1Tablet, CoatedOralPrecision Dose, Inc.68094-589

Free account

Keep searching with a free account

You’ve used your 3 free searches for this session. Log in or create a free Med-Code account to keep looking up NDCs, J-codes and drugs.

Create a free accountLog in