Gabapentin
- Product NDC
- 71205-766
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Gabapentin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA204989
- Marketing category
- ANDA
- Substance
- GABAPENTIN
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 71205-766-14 | 14 CAPSULE in 1 BOTTLE, PLASTIC (71205-766-14) | 2024-03-20 | | No | Historical |
| 71205-766-30 | 30 CAPSULE in 1 BOTTLE, PLASTIC (71205-766-30) | 2023-02-21 | | No | Historical |
| 71205-766-60 | 60 CAPSULE in 1 BOTTLE, PLASTIC (71205-766-60) | 2023-02-21 | | No | Historical |
| 71205-766-90 | 90 CAPSULE in 1 BOTTLE, PLASTIC (71205-766-90) | 2023-02-21 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Gabapentin | Proficient Rx LP | 2024-03-01 | HUMAN PRESCRIPTION DRUG LABEL | 2 |