Gabapentin
- Product NDC
- 60760-741
- 11-digit product format
- 607600741
- Labeler code
- 60760
- Product ID
- 60760-741_2b49cecc-6442-8870-e063-6294a90a61b9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Gabapentin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- St. Mary's Medical Park Pharmacy
- Application
- ANDA204989
- Marketing category
- ANDA
- Marketing start
- 2020-12-22
- Substance
- GABAPENTIN
- Active strength
- 300 mg/1
- Pharmacologic classes
- 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 |
|---|
| 60760-741-60 | 60760074160 | 60 CAPSULE in 1 BOTTLE, PLASTIC (60760-741-60) | 60 capsule | 2020-12-22 | No | No | Historical |
| 60760-741-90 | 60760074190 | 90 CAPSULE in 1 BOTTLE, PLASTIC (60760-741-90) | 90 capsule | 2020-12-22 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Gabapentin | St. Mary's Medical Park Pharmacy | 2025-01-09 | HUMAN PRESCRIPTION DRUG LABEL | 2 |