Gabapentin
- Product NDC
- 55154-6846
- 11-digit product format
- 551546846
- Labeler code
- 55154
- Product ID
- 55154-6846_26da19f9-f0fe-4d61-9094-c4bfad694156
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Gabapentin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Cardinal Health
- Application
- ANDA078428
- Marketing category
- ANDA
- Marketing start
- 2009-11-24
- 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
- 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 |
|---|
| 55154-6846-0 | 55154684600 | 10 BLISTER PACK in 1 BAG (55154-6846-0) > 1 CAPSULE in 1 BLISTER PACK | 10 blister pack | 2009-11-24 | 0000-00-00 | No | No | Current |