Gabapentin
- Product NDC
- 71335-1323
- 11-digit product format
- 713351323
- Labeler code
- 71335
- Product ID
- 71335-1323_bb87b2ea-4c7d-4194-bc48-ec16b1e9d96a
- 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
- Marketing end
- 0000-00-00
- Substance
- GABAPENTIN
- Active strength
- 300 mg/1
- Pharmacologic classes
- Anti-epileptic Agent [EPC], Decreased Central Nervous System Disorganized Electrical Activity [PE]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 71335-1323-1 | 71335132301 | 30 CAPSULE in 1 BOTTLE (71335-1323-1) | 30 capsule | 2019-09-03 | 0000-00-00 | No | No | Current |
| 71335-1323-2 | 71335132302 | 90 CAPSULE in 1 BOTTLE (71335-1323-2) | 90 capsule | 2019-09-03 | 0000-00-00 | No | No | Current |