Gabapentin
- Product NDC
- 71205-671
- 11-digit product format
- 712050671
- Labeler code
- 71205
- Product ID
- 71205-671_41f58323-3405-499a-a301-dfcc0f6b5a5d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Gabapentin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA204989
- Marketing category
- ANDA
- Marketing start
- 2016-02-18
- Substance
- GABAPENTIN
- Active strength
- 400 mg/1
- Pharmacologic classes
- Anti-epileptic Agent [EPC], Decreased Central Nervous System Disorganized Electrical Activity [PE]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 6CW7F3G59X | GABAPENTIN | 60142-96-3 | GABAPENTIN |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71205-671-30 | 71205067130 | 30 CAPSULE in 1 BOTTLE, PLASTIC (71205-671-30) | 30 capsule | 2022-06-24 | No | No | Historical |
| 71205-671-60 | 71205067160 | 60 CAPSULE in 1 BOTTLE, PLASTIC (71205-671-60) | 60 capsule | 2022-06-24 | No | No | Historical |
| 71205-671-72 | 71205067172 | 120 CAPSULE in 1 BOTTLE, PLASTIC (71205-671-72) | 120 capsule | 2022-06-24 | No | No | Historical |
| 71205-671-90 | 71205067190 | 90 CAPSULE in 1 BOTTLE, PLASTIC (71205-671-90) | 90 capsule | 2022-06-24 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Gabapentin | Proficient Rx LP | 2023-01-01 | HUMAN PRESCRIPTION DRUG LABEL | 3 |