Gabapentin
- Product NDC
- 70934-950
- 11-digit product format
- 709340950
- Labeler code
- 70934
- Product ID
- 70934-950_d815ef8e-23ca-0be2-e053-2995a90a504b
- 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
- 2022-02-15
- Marketing end
- 0000-00-00
- Substance
- GABAPENTIN
- Active strength
- 800 mg/1
- Pharmacologic classes
- Anti-epileptic Agent [EPC], Decreased Central Nervous System Disorganized Electrical Activity [PE]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 70934-950-30 | 70934095030 | 30 TABLET in 1 BOTTLE, PLASTIC (70934-950-30) | 30 tablet | 2022-02-15 | 0000-00-00 | No | No | Current |