Gabapentin
- Product NDC
- 42708-056
- 11-digit product format
- 427080056
- Labeler code
- 42708
- Product ID
- 42708-056_a9179a9a-b5f6-4ac8-931f-49856bc8270a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Gabapentin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- QPharma Inc
- Application
- ANDA090858
- Marketing category
- ANDA
- Marketing start
- 2016-05-06
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#