Gabapentin
- Product NDC
- 69367-134
- 11-digit product format
- 693670134
- Labeler code
- 69367
- Product ID
- 69367-134_1647af99-e383-471a-a4fd-15dad8bfc4e3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Gabapentin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Westminster Pharmaceuticals, LLC
- Application
- ANDA205101
- Marketing category
- ANDA
- Marketing start
- 2016-04-11
- 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 Product Concepts#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69367-134 | GABAPENTIN TABLET [WESTMINSTER PHARMACEUTICALS, LLC] | 10 | Legacy NDC | 20250417_303b46df-64f7-20c1-e054-00144ff88e88.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 69367-134-03 | 69367013403 | 90 TABLET in 1 BOTTLE (69367-134-03) | 90 tablet | 2016-04-11 | 0000-00-00 | No | No | Current |
| 69367-134-04 | 69367013404 | 100 TABLET in 1 BOTTLE (69367-134-04) | 100 tablet | 2018-04-30 | 0000-00-00 | No | No | Current |
| 69367-134-06 | 69367013406 | 500 TABLET in 1 BOTTLE (69367-134-06) | 500 tablet | 2016-04-11 | 0000-00-00 | No | No | Current |