Gabapentin
- Product NDC
- 71205-514
- 11-digit product format
- 712050514
- Labeler code
- 71205
- Product ID
- 71205-514_dca73902-4c06-4304-a5a4-b289b020cee4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Gabapentin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA205101
- Marketing category
- ANDA
- Marketing start
- 2016-02-04
- Substance
- GABAPENTIN
- Active strength
- 800 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 |
|---|
| 71205-514-30 | 71205051430 | 30 TABLET in 1 BOTTLE (71205-514-30) | 30 tablet | 2020-12-09 | No | No | Historical |
| 71205-514-60 | 71205051460 | 60 TABLET in 1 BOTTLE (71205-514-60) | 60 tablet | 2020-12-09 | No | No | Historical |
| 71205-514-90 | 71205051490 | 90 TABLET in 1 BOTTLE (71205-514-90) | 90 tablet | 2020-12-09 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Gabapentin | Proficient Rx LP | 2022-04-01 | HUMAN PRESCRIPTION DRUG LABEL | 2 |