Gabapentin
- Product NDC
- 70518-0810
- 11-digit product format
- 705180810
- Labeler code
- 70518
- Product ID
- 70518-0810_e26e073b-5645-3670-e053-2a95a90a8ab3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- GABAPENTIN
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA203244
- Marketing category
- ANDA
- Marketing start
- 2017-10-30
- 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
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-0810 | GABAPENTIN TABLET, FILM COATED [REMEDYREPACK INC.] | 9 | Legacy NDC | 20220628_8ededc3f-bf92-463d-bf89-ef10e38639a9.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-0810-0 | 70518081000 | 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-0810-0) | 2017-10-30 | 0000-00-00 | No | No | Current |
| 70518-0810-1 | 70518081001 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0810-1) | 2017-12-04 | 0000-00-00 | No | No | Current |
| 70518-0810-2 | 70518081002 | 180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0810-2) | 2018-01-22 | 0000-00-00 | No | No | Current |