Gabapentin
- Product NDC
- 49999-799
- 11-digit product format
- 499990799
- Labeler code
- 49999
- Product ID
- 49999-799_77f1cb91-9dab-4546-a229-1b1b1b4194eb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Gabapentin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Quality Care Products, LLC
- Application
- ANDA077662
- Marketing category
- ANDA
- Marketing start
- 2010-12-06
- Marketing end
- 0000-00-00
- Substance
- GABAPENTIN
- Active strength
- 800 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