Gabapentin
- Product NDC
- 55154-7131
- 11-digit product format
- 551547131
- Labeler code
- 55154
- Product ID
- 55154-7131_28cca494-3ca0-4b0f-b262-0fe612d44b37
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Gabapentin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Cardinal Health
- Application
- ANDA075350
- Marketing category
- ANDA
- Marketing start
- 2014-08-12
- Marketing end
- 0000-00-00
- Substance
- GABAPENTIN
- Active strength
- 100 mg/1
- Pharmacologic classes
- Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 55154-7131-0 | 55154713100 | 10 BLISTER PACK in 1 BAG (55154-7131-0) > 1 CAPSULE in 1 BLISTER PACK | 10 blister pack | 2014-08-12 | 0000-00-00 | No | No | Current |