NDC codes

FDA NDC Directory
Product NDC (as listed)71335-1132Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71335-1132Add 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
71335-1132-07133511320028 TABLET, FILM COATED in 1 BOTTLE (71335-1132-0)Marketed from Apr 2, 2024
71335-1132-17133511320130 TABLET, FILM COATED in 1 BOTTLE (71335-1132-1)Marketed from Sep 18, 2019
71335-1132-27133511320260 TABLET, FILM COATED in 1 BOTTLE (71335-1132-2)Marketed from Mar 22, 2019
71335-1132-371335113203180 TABLET, FILM COATED in 1 BOTTLE (71335-1132-3)Marketed from Mar 24, 2020
71335-1132-47133511320490 TABLET, FILM COATED in 1 BOTTLE (71335-1132-4)Marketed from Mar 21, 2019
71335-1132-571335113205100 TABLET, FILM COATED in 1 BOTTLE (71335-1132-5)Marketed from Apr 2, 2024
71335-1132-671335113206120 TABLET, FILM COATED in 1 BOTTLE (71335-1132-6)Marketed from Apr 5, 2019
71335-1132-771335113207500 TABLET, FILM COATED in 1 BOTTLE (71335-1132-7)Marketed from Apr 2, 2024
71335-1132-87133511320884 TABLET, FILM COATED in 1 BOTTLE (71335-1132-8)Marketed from Apr 2, 2024
71335-1132-971335113209112 TABLET, FILM COATED in 1 BOTTLE (71335-1132-9)Marketed from Apr 2, 2024

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, Film coated
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 203244
Marketing start
Listing expires
Other FDA classes
Decreased Central Nervous System Disorganized Electrical Activity (Physiologic effect)
Identifiers
Product ID 71335-1132_b600479a-315e-47e3-9c50-bfaab1d5c12cSPL ID b600479a-315e-47e3-9c50-bfaab1d5c12cSPL set ID c9944562-563a-423d-972c-f0313375d234RxCUI 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

N471335113200 followed by a unit qualifier and the quantity

Package 71335-1132-00. 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 tablets are 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 tablets are 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 203244

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

FDA NDC Directory listings under ANDA 203244
ProductStrengthForm · routeLabelerProduct NDC
GabapentinGabapentin 800 mg/1Tablet, Film coatedOralAphena Pharma Solutions - Tennessee, LLC71610-426
GabapentinGabapentin 600 mg/1Tablet, Film coatedOralBryant Ranch Prepack72162-2141
GabapentinGabapentin 800 mg/1Tablet, Film coatedOralBryant Ranch Prepack72162-2142
GabapentinGabapentin 600 mg/1Tablet, Film coatedOralREMEDYREPACK INC.70518-2098
GabapentinGabapentin 600 mg/1Tablet, Film coatedOralAphena Pharma Solutions - Tennessee, LLC71610-044
GabapentinGabapentin 800 mg/1Tablet, Film coatedOralBryant Ranch Prepack71335-1007
GabapentinGabapentin 600 mg/1Tablet, Film coatedOralBryant Ranch Prepack71335-1026
GabapentinGabapentin 600 mg/1TabletOralStrides Pharma Science Limited64380-727
GabapentinGabapentin 800 mg/1TabletOralStrides Pharma Science Limited64380-728
GabapentinGabapentin 800 mg/1Tablet, Film coatedOralBryant Ranch Prepack71335-1041
GabapentinGabapentin 800 mg/1Tablet, Film coatedOralDIRECT RX72189-158
GabapentinGabapentin 600 mg/1Tablet, Film coatedOralProficient Rx LP71205-457
GabapentinGabapentin 800 mg/1Tablet, Film coatedOralProficient Rx LP71205-160
GabapentinGabapentin 800 mg/1Tablet, Film coatedOralBryant Ranch Prepack71335-1601
GabapentinGabapentin 600 mg/1Tablet, Film coatedOralSt. Mary's Medical Park Pharmacy60760-066

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