Gabapentin
- Product NDC
- 0904-5631
- 11-digit product format
- 009045631
- Labeler code
- 0904
- Product ID
- 0904-5631_d2dd7fa1-6756-474d-8eb9-10efed51dfdf
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Gabapentin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Major Pharmaceuticals
- Application
- ANDA075360
- Marketing category
- ANDA
- Marketing start
- 2005-04-06
- Marketing end
- 2019-07-31
- 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
- 0000-00-00
- Current FDA listing
- Historical FDA.report record