Gabapentin
- Product NDC
- 55154-7132
- 11-digit product format
- 551547132
- Labeler code
- 55154
- Product ID
- 55154-7132_e21100ce-0656-4580-bf7a-f49b5a018614
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Gabapentin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Cardinal Health
- Application
- ANDA078926
- Marketing category
- ANDA
- Marketing start
- 2014-11-03
- Marketing end
- 2021-06-30
- 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
- 0000-00-00
- 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 |
|---|
| 55154-7132-0 | 55154713200 | 10 BLISTER PACK in 1 BAG (55154-7132-0) > 1 TABLET, FILM COATED in 1 BLISTER PACK | 10 blister pack | 2014-11-03 | 2021-06-30 | No | No | Current |