GABAPENTIN
- Product NDC
- 60760-837
- 11-digit product format
- 607600837
- Labeler code
- 60760
- Product ID
- 60760-837_4ddc1bc7-5ca0-f979-e063-6294a90a2422
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Gabapentin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- ST. MARY'S MEDICAL PARK PHARMACY
- Application
- ANDA214957
- Marketing category
- ANDA
- Marketing start
- 2021-10-01
- Substance
- GABAPENTIN
- Active strength
- 800 mg/1
- Pharmacologic classes
- Decreased Central Nervous System Disorganized Electrical Activity [PE]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- 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 |
|---|
| 60760-837-60 | 60760083760 | 60 TABLET in 1 BOTTLE, PLASTIC (60760-837-60) | 60 tablet | 2026-03-18 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| GABAPENTIN | ST. MARY'S MEDICAL PARK PHARMACY | 2026-03-25 | HUMAN PRESCRIPTION DRUG LABEL | 1 |