Gabapentin
- Product NDC
- 67544-353
- 11-digit product format
- 675440353
- Labeler code
- 67544
- Product ID
- 67544-353_03cba200-f94b-4357-bee2-b32b12f19891
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Gabapentin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Application
- ANDA075350
- Marketing category
- ANDA
- Marketing start
- 2004-10-04
- Marketing end
- 0000-00-00
- Substance
- GABAPENTIN
- Active strength
- 300 mg/1
- Pharmacologic classes
- Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record