Gabapentin
- Product NDC
- 70934-593
- 11-digit product format
- 709340593
- Labeler code
- 70934
- Product ID
- 70934-593_cd4faec4-7ee4-3150-e053-2a95a90add00
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- GABAPENTIN
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals
- Application
- ANDA203244
- Marketing category
- ANDA
- Marketing start
- 2021-03-01
- 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70934-593-30 | 70934059330 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-593-30) | 2021-09-28 | 0000-00-00 | No | No | Current |
| 70934-593-90 | 70934059390 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-593-90) | 2021-03-01 | 0000-00-00 | No | No | Current |