Neurontin
- Product NDC
- 70518-1405
- 11-digit product format
- 705181405
- Labeler code
- 70518
- Product ID
- 70518-1405_92bcbb6b-7936-7ae8-e053-2a95a90a7c3d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- gabapentin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- NDA020235
- Marketing category
- NDA
- Marketing start
- 2018-09-07
- 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