Prescription drug · ANDA
Gabapentin NDC 72737-005
Gabapentin 100 mg/1 · Capsule · Oral · STALLION LABORATORIES PRIVATE LIMITED
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 72737-005-01 | 7273700050172737000501 | 30 CAPSULE in 1 BOTTLE (72737-005-01)Marketed from Aug 7, 2025 | |
| 72737-005-02 | 7273700050272737000502 | 100 CAPSULE in 1 BOTTLE (72737-005-02)Marketed from Aug 7, 2025 | |
| 72737-005-03 | 7273700050372737000503 | 500 CAPSULE in 1 BOTTLE (72737-005-03)Marketed from Aug 7, 2025 | |
| 72737-005-04 | 7273700050472737000504 | 1000 CAPSULE in 1 BOTTLE (72737-005-04)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 — 100 mg/1
- Dosage form
- Capsule
- Route
- Oral
- Labeler
- STALLION LABORATORIES PRIVATE LIMITEDNDC labeler code 72737
- 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 72737-005_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
N472737000501followed by a unit qualifier and the quantityPackage 72737-0005-01. 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.
About NDC 72737-005
- What is NDC 72737-005?
- 72737-005 is the product NDC for Gabapentin, Gabapentin 100 mg/1 capsule, listed with the FDA by STALLION LABORATORIES PRIVATE LIMITED. 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?
- STALLION LABORATORIES PRIVATE LIMITED, NDC labeler code 72737. 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.
Related NDCs: other Gabapentin products
Other finished products listed under the same name: strengths, forms and labelers.
| 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 | 70518-4740-0070518-4740-01 |
| 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 |
Other NDCs under ANDA 219319
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.
| Product | Strength | Form · route | Labeler | Product NDC |
|---|---|---|---|---|
| Gabapentin | Gabapentin 100 mg/1 | CapsuleOral | Amici Pharma, Inc. | 69292-640 |
| Gabapentin | Gabapentin 300 mg/1 | CapsuleOral | Amici Pharma, Inc. | 69292-641 |
| Gabapentin | Gabapentin 400 mg/1 | CapsuleOral | Amici Pharma, Inc. | 69292-642 |
| Gabapentin | Gabapentin 300 mg/1 | CapsuleOral | STALLION LABORATORIES PRIVATE LIMITED | 72737-006 |
| Gabapentin | Gabapentin 400 mg/1 | CapsuleOral | STALLION LABORATORIES PRIVATE LIMITED | 72737-007 |
| Gabapentin | Gabapentin 200 mg/1 | CapsuleOral | Pangea Pharmaceuticals, LLC | 81279-126 |