Gabapentin
- Product NDC
- 55700-815
- 11-digit product format
- 557000815
- Labeler code
- 55700
- Product ID
- 55700-815_0efcbe2d-6cb3-428c-b051-da4531493a71
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- GABAPENTIN
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Quality Care Products, LLC
- Application
- ANDA203244
- Marketing category
- ANDA
- Marketing start
- 2019-11-08
- 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 |
|---|
| 55700-815 | GABAPENTIN TABLET, FILM COATED [QUALITY CARE PRODUCTS, LLC] | 11 | Legacy NDC | 20241220_ff1801c6-e1d2-4a30-aa38-7382102ec125.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55700-815-30 | 55700081530 | 30 TABLET, FILM COATED in 1 BOTTLE (55700-815-30) | 2019-11-08 | 0000-00-00 | No | No | Current |
| 55700-815-60 | 55700081560 | 60 TABLET, FILM COATED in 1 BOTTLE (55700-815-60) | 2019-11-08 | 0000-00-00 | No | No | Current |
| 55700-815-90 | 55700081590 | 90 TABLET, FILM COATED in 1 BOTTLE (55700-815-90) | 2019-11-08 | 0000-00-00 | No | No | Current |