GABAPENTIN
- Product NDC
- 43602-466
- 11-digit product format
- 436020466
- Labeler code
- 43602
- Product ID
- 43602-466_dc5d1f9f-b231-4320-aade-f051a8f4deed
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Gabapentin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Ascent Pharmaceuticals, Inc
- Application
- ANDA214957
- Marketing category
- ANDA
- Marketing start
- 2021-10-01
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 43602-466 | GABAPENTIN TABLET [ASCENT PHARMACEUTICALS, INC] | 3 | Legacy NDC | 20211008_11580370-55dd-4b61-b051-68b49f6fd2ea.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 43602-466-05 | 43602046605 | 500 TABLET in 1 BOTTLE (43602-466-05) | 500 tablet | 2021-10-01 | 0000-00-00 | No | No | Current |
| 43602-466-30 | 43602046630 | 30 TABLET in 1 BOTTLE (43602-466-30) | 30 tablet | 2021-10-01 | 0000-00-00 | No | No | Current |