NDC codes

FDA NDC Directory
Product NDC (as listed)72737-006Labeler and product segments. Claims need a package NDC.
Product NDC at billing width72737-0006Add 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
72737-006-017273700060130 CAPSULE in 1 BOTTLE (72737-006-01)Marketed from Aug 7, 2025
72737-006-0272737000602100 CAPSULE in 1 BOTTLE (72737-006-02)Marketed from Aug 7, 2025
72737-006-0372737000603500 CAPSULE in 1 BOTTLE (72737-006-03)Marketed from Aug 7, 2025
72737-006-04727370006041000 CAPSULE in 1 BOTTLE (72737-006-04)Marketed from Aug 7, 2025

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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 — 300 mg/1
Dosage form
Capsule
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 219319
Marketing start
Listing expires
Other FDA classes
Decreased Central Nervous System Disorganized Electrical Activity (Physiologic effect)
Identifiers
Product ID 72737-006_30d4f239-f37b-4b6e-b25e-043a33489011SPL ID 30d4f239-f37b-4b6e-b25e-043a33489011SPL set ID b26fd0c6-6aab-4957-8a32-cc7adb9b5fc9RxCUI 310430, 310431, 310432UNII 6CW7F3G59XUPC 0372737007028, 0372737006021, 0372737005024

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

N472737000601 followed by a unit qualifier and the quantity

Package 72737-0006-01. 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 .

Indications (excerpt from the label)

Gabapentin capsules 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 capsules 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 219319

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

FDA NDC Directory listings under ANDA 219319
ProductStrengthForm · routeLabelerProduct NDC
GabapentinGabapentin 400 mg/1CapsuleOralAmici Pharma, Inc.69292-642
GabapentinGabapentin 100 mg/1CapsuleOralAmici Pharma, Inc.69292-640
GabapentinGabapentin 300 mg/1CapsuleOralAmici Pharma, Inc.69292-641
GabapentinGabapentin 100 mg/1CapsuleOralSTALLION LABORATORIES PRIVATE LIMITED72737-005
GabapentinGabapentin 400 mg/1CapsuleOralSTALLION LABORATORIES PRIVATE LIMITED72737-007
GabapentinGabapentin 200 mg/1CapsuleOralPangea Pharmaceuticals, LLC81279-126

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