GABAPENTIN
- Product NDC
- 50268-351
- 11-digit product format
- 502680351
- Labeler code
- 50268
- Product ID
- 50268-351_e87e2c26-cd78-ee2a-e053-2995a90aaef9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- gabapentin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- AvPAK
- Application
- ANDA202764
- Marketing category
- ANDA
- Marketing start
- 2015-02-13
- Marketing end
- 0000-00-00
- Substance
- GABAPENTIN
- Active strength
- 600 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 |
|---|
| 50268-351-15 | 50268035115 | 50 BLISTER PACK in 1 BOX (50268-351-15) > 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-351-11) | 50 blister pack | 2015-02-13 | 0000-00-00 | No | No | Current |