Gabapentin
- Product NDC
- 42291-300
- 11-digit product format
- 422910300
- Labeler code
- 42291
- Product ID
- 42291-300_7354472d-acb4-4817-e053-2a91aa0a08c6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Gabapentin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- AvKARE, Inc.
- Application
- ANDA078428
- Marketing category
- ANDA
- Marketing start
- 2018-08-15
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record