Gabapentin
- Product NDC
- 42291-301
- 11-digit product format
- 422910301
- Labeler code
- 42291
- Product ID
- 42291-301_d57a9bfb-0865-244c-e053-2a95a90a1253
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Gabapentin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- AvKARE
- Application
- ANDA078428
- Marketing category
- ANDA
- Marketing start
- 2018-08-15
- 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 table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 42291-301-50 | 42291030150 | 500 CAPSULE in 1 BOTTLE (42291-301-50) | 500 capsule | 2018-08-15 | 0000-00-00 | No | No | Current |