Gabapentin
- Product NDC
- 68071-1995
- 11-digit product format
- 680711995
- Labeler code
- 68071
- Product ID
- 68071-1995_7cc540e1-634e-2473-e053-2991aa0a4466
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Gabapentin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- Application
- ANDA075350
- Marketing category
- ANDA
- Marketing start
- 2014-03-17
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record