Gabapentin
- Product NDC
- 50090-3915
- 11-digit product format
- 500903915
- Labeler code
- 50090
- Product ID
- 50090-3915_29c82f4d-67a6-4357-bc28-223aeab90c94
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Gabapentin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA078926
- Marketing category
- ANDA
- Marketing start
- 2012-10-16
- Marketing end
- 0000-00-00
- Substance
- GABAPENTIN
- Active strength
- 600 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#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-3915-0 | 50090391500 | 90 TABLET, FILM COATED in 1 BOTTLE (50090-3915-0) | 2018-12-06 | 0000-00-00 | No | No | Current |
| 50090-3915-1 | 50090391501 | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50090-3915-1) | 2014-11-28 | 0000-00-00 | No | No | Current |
| 50090-3915-2 | 50090391502 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50090-3915-2) | 2014-11-28 | 0000-00-00 | No | No | Current |