Gabapentin
- Product NDC
- 70934-933
- 11-digit product format
- 709340933
- Labeler code
- 70934
- Product ID
- 70934-933_d39a6bdb-2c3e-4808-e053-2995a90a64cb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Gabapentin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals
- Application
- ANDA206402
- Marketing category
- ANDA
- Marketing start
- 2021-12-08
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70934-933-90 | 70934093390 | 90 TABLET in 1 BOTTLE, PLASTIC (70934-933-90) | 90 tablet | 2021-12-08 | 0000-00-00 | No | No | Current |