Gabapentin
- Product NDC
- 71335-1497
- 11-digit product format
- 713351497
- Labeler code
- 71335
- Product ID
- 71335-1497_204c96af-0d7b-4ff8-ab04-3678b1831854
- 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
- 400 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 table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71335-1497-1 | 71335149701 | 90 CAPSULE in 1 BOTTLE (71335-1497-1) | 90 capsule | 2022-02-09 | 0000-00-00 | No | No | Current |
| 71335-1497-2 | 71335149702 | 28 CAPSULE in 1 BOTTLE (71335-1497-2) | 28 capsule | 2022-02-09 | 0000-00-00 | No | No | Current |
| 71335-1497-3 | 71335149703 | 120 CAPSULE in 1 BOTTLE (71335-1497-3) | 120 capsule | 2022-02-09 | 0000-00-00 | No | No | Current |
| 71335-1497-4 | 71335149704 | 30 CAPSULE in 1 BOTTLE (71335-1497-4) | 30 capsule | 2022-02-09 | 0000-00-00 | No | No | Current |
| 71335-1497-5 | 71335149705 | 60 CAPSULE in 1 BOTTLE (71335-1497-5) | 60 capsule | 2022-02-09 | 0000-00-00 | No | No | Current |