Gabapentin
- Product NDC
- 59115-073
- 11-digit product format
- 591150073
- Labeler code
- 59115
- Product ID
- 59115-073_644343c6-5cd6-435f-a260-0d62901b3b87
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Gabapentin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Hikma Pharmaceutical
- Application
- ANDA078150
- Marketing category
- ANDA
- Marketing start
- 2007-07-09
- 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