Gabapentin
- Product NDC
- 72162-2140
- 11-digit product format
- 721622140
- Labeler code
- 72162
- Product ID
- 72162-2140_5734a653-53ce-4850-9c6d-c426d9899846
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Gabapentin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA206943
- Marketing category
- ANDA
- Marketing start
- 2018-05-14
- Substance
- GABAPENTIN
- Active strength
- 400 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 |
|---|
| 72162-2140-1 | 72162214001 | 100 CAPSULE in 1 BOTTLE, PLASTIC (72162-2140-1) | 100 capsule | 2023-10-12 | No | No | Historical |
| 72162-2140-5 | 72162214005 | 500 CAPSULE in 1 BOTTLE, PLASTIC (72162-2140-5) | 500 capsule | 2023-10-12 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Gabapentin | Bryant Ranch Prepack | 2023-12-20 | HUMAN PRESCRIPTION DRUG LABEL | 101 |