Gabapentin
- Product NDC
- 70518-2960
- 11-digit product format
- 705182960
- Labeler code
- 70518
- Product ID
- 70518-2960_e7b36b40-509b-77e5-e053-2995a90a6e7c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Gabapentin
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA207057
- Marketing category
- ANDA
- Marketing start
- 2020-12-07
- 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
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-2960 | GABAPENTIN TABLET, COATED [REMEDYREPACK INC.] | 9 | Legacy NDC | 20250406_e14f4365-2728-4a9d-b07a-3929d5dd20e2.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2960-0 | 70518296000 | 28 TABLET, COATED in 1 BLISTER PACK (70518-2960-0) | 2020-12-07 | 0000-00-00 | No | No | Current |
| 70518-2960-1 | 70518296001 | 30 TABLET, COATED in 1 BLISTER PACK (70518-2960-1) | 2021-05-04 | 0000-00-00 | No | No | Current |
| 70518-2960-2 | 70518296002 | 90 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-2960-2) | 2022-07-29 | 0000-00-00 | No | No | Current |