Gabapentin
- Product NDC
- 70518-1160
- 11-digit product format
- 705181160
- Labeler code
- 70518
- Product ID
- 70518-1160_e3146524-84bd-703a-e053-2995a90a1cb3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- GABAPENTIN
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA203244
- Marketing category
- ANDA
- Marketing start
- 2018-05-07
- 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
- 2023-12-31
- 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 |
|---|
| 70518-1160-1 | 70518116001 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1160-1) | 2019-02-08 | 0000-00-00 | No | No | Current |