Gabapentin
- Product NDC
- 0143-3994
- 11-digit product format
- 001433994
- Labeler code
- 0143
- Product ID
- 0143-3994_164477b7-26bf-4c39-b2ac-d086ec30a07d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Gabapentin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- West-ward Pharmaceutical Corp
- Application
- ANDA078150
- Marketing category
- ANDA
- Marketing start
- 2007-07-09
- 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
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record