NDC codes

FDA NDC Directory
Product NDC (as listed)71335-1200Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71335-1200Add 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
71335-1200-07133512000028 TABLET in 1 BOTTLE (71335-1200-0)Marketed from Jan 30, 2025
71335-1200-17133512000130 TABLET in 1 BOTTLE (71335-1200-1)Marketed from May 6, 2019
71335-1200-27133512000260 TABLET in 1 BOTTLE (71335-1200-2)Marketed from May 13, 2019
71335-1200-371335120003180 TABLET in 1 BOTTLE (71335-1200-3)Marketed from Jun 12, 2019
71335-1200-47133512000490 TABLET in 1 BOTTLE (71335-1200-4)Marketed from Apr 22, 2019
71335-1200-571335120005100 TABLET in 1 BOTTLE (71335-1200-5)Marketed from Jan 30, 2025
71335-1200-671335120006120 TABLET in 1 BOTTLE (71335-1200-6)Marketed from May 2, 2019
71335-1200-771335120007500 TABLET in 1 BOTTLE (71335-1200-7)Marketed from Jan 30, 2025
71335-1200-87133512000884 TABLET in 1 BOTTLE (71335-1200-8)Marketed from Jan 30, 2025
71335-1200-971335120009112 TABLET in 1 BOTTLE (71335-1200-9)Marketed from Jan 30, 2025

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
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 206402
Marketing start
Listing expires
Other FDA classes
Decreased Central Nervous System Disorganized Electrical Activity (Physiologic effect)
Identifiers
Product ID 71335-1200_4be0d60b-e4d2-484b-a870-6fdc3893f5f9SPL ID 4be0d60b-e4d2-484b-a870-6fdc3893f5f9SPL set ID a1ff94a9-69c4-486a-aab2-563c7ed244c8RxCUI 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

N471335120000 followed by a unit qualifier and the quantity

Package 71335-1200-00. 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 206402

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

FDA NDC Directory listings under ANDA 206402
ProductStrengthForm · routeLabelerProduct NDC
GabapentinGabapentin 600 mg/1TabletOralREMEDYREPACK INC.70518-2842
GabapentinGabapentin 800 mg/1TabletOralBryant Ranch Prepack71335-2037
GabapentinGabapentin 800 mg/1TabletOralDirect_Rx72189-619
GabapentinGabapentin 800 mg/1TabletOralBryant Ranch Prepack71335-2038
GabapentinGabapentin 800 mg/1TabletOralAscend Laboratories, LLC67877-429
GabapentinGabapentin 600 mg/1TabletOralAscend Laboratories, LLC67877-428
GabapentinGabapentin 800 mg/1TabletOralREMEDYREPACK INC.70518-2912
GabapentinGabapentin 600 mg/1TabletOralBryant Ranch Prepack71335-2048
GabapentinGabapentin 800 mg/1TabletOralAdvanced Rx of Tennessee, LLC80425-0035
GabapentinGabapentin 800 mg/1TabletOralNuCare Pharmaceuticals, Inc.68071-5310
GabapentinGabapentin 600 mg/1TabletOralBryant Ranch Prepack71335-2281

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