Prescription drug · ANDA
Gabapentin NDC 64380-727
Gabapentin 600 mg/1 · Tablet · Oral · Strides Pharma Science Limited
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 64380-727-01 | 64380072701 | 100 TABLET in 1 CONTAINER (64380-727-01)Marketed from Nov 10, 2025 | |
| 64380-727-02 | 64380072702 | 500 TABLET in 1 CONTAINER (64380-727-02)Marketed from Nov 10, 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 — 600 mg/1
- Dosage form
- Tablet
- 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 64380-727_a4928566-6bc9-4a2a-a368-c68afc402368SPL ID a4928566-6bc9-4a2a-a368-c68afc402368SPL set ID bec31452-b52b-4698-ba4c-0b614780ee84RxCUI 310433, 310434UNII 6CW7F3G59XUPC 0364380728016, 0364380727019
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
N464380072701followed by a unit qualifier and the quantityPackage 64380-0727-01. 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
Label details couldn’t be retrieved right now. Open the label on DailyMed.
Other NDCs under ANDA 203244
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 800 mg/1 | Tablet, Film coatedOral | Aphena Pharma Solutions - Tennessee, LLC | 71610-426 |
| Gabapentin | Gabapentin 600 mg/1 | Tablet, Film coatedOral | Bryant Ranch Prepack | 72162-2141 |
| Gabapentin | Gabapentin 800 mg/1 | Tablet, Film coatedOral | Bryant Ranch Prepack | 72162-2142 |
| Gabapentin | Gabapentin 600 mg/1 | Tablet, Film coatedOral | REMEDYREPACK INC. | 70518-2098 |
| Gabapentin | Gabapentin 600 mg/1 | Tablet, Film coatedOral | Aphena Pharma Solutions - Tennessee, LLC | 71610-044 |
| Gabapentin | Gabapentin 800 mg/1 | Tablet, Film coatedOral | Bryant Ranch Prepack | 71335-1007 |
| Gabapentin | Gabapentin 600 mg/1 | Tablet, Film coatedOral | Bryant Ranch Prepack | 71335-1026 |
| Gabapentin | Gabapentin 800 mg/1 | TabletOral | Strides Pharma Science Limited | 64380-728 |
| Gabapentin | Gabapentin 800 mg/1 | Tablet, Film coatedOral | Bryant Ranch Prepack | 71335-1041 |
| Gabapentin | Gabapentin 800 mg/1 | Tablet, Film coatedOral | DIRECT RX | 72189-158 |
| Gabapentin | Gabapentin 600 mg/1 | Tablet, Film coatedOral | Bryant Ranch Prepack | 71335-1132 |
| Gabapentin | Gabapentin 600 mg/1 | Tablet, Film coatedOral | Proficient Rx LP | 71205-457 |
| Gabapentin | Gabapentin 800 mg/1 | Tablet, Film coatedOral | Proficient Rx LP | 71205-160 |
| Gabapentin | Gabapentin 800 mg/1 | Tablet, Film coatedOral | Bryant Ranch Prepack | 71335-1601 |
| Gabapentin | Gabapentin 600 mg/1 | Tablet, Film coatedOral | St. Mary's Medical Park Pharmacy | 60760-066 |