GABAPENTIN
- Product NDC
- 43063-756
- 11-digit product format
- 430630756
- Labeler code
- 43063
- Product ID
- 43063-756_d2bb8d09-196e-963a-e053-2a95a90a430c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- GABAPENTIN
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA205101
- Marketing category
- ANDA
- Marketing start
- 2016-11-20
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 43063-756-30 | 43063075630 | 30 TABLET in 1 BOTTLE, PLASTIC (43063-756-30) | 30 tablet | 2017-04-24 | 0000-00-00 | No | No | Current |
| 43063-756-60 | 43063075660 | 60 TABLET in 1 BOTTLE, PLASTIC (43063-756-60) | 60 tablet | 2017-04-24 | 0000-00-00 | No | No | Current |
| 43063-756-83 | 43063075683 | 540 TABLET in 1 BOTTLE, PLASTIC (43063-756-83) | 540 tablet | 2017-04-24 | 0000-00-00 | No | No | Current |
| 43063-756-86 | 43063075686 | 360 TABLET in 1 BOTTLE, PLASTIC (43063-756-86) | 360 tablet | 2017-04-24 | 0000-00-00 | No | No | Current |
| 43063-756-90 | 43063075690 | 90 TABLET in 1 BOTTLE, PLASTIC (43063-756-90) | 90 tablet | 2017-04-24 | 0000-00-00 | No | No | Current |
| 43063-756-93 | 43063075693 | 180 TABLET in 1 BOTTLE, PLASTIC (43063-756-93) | 180 tablet | 2017-04-24 | 0000-00-00 | No | No | Current |
| 43063-756-94 | 43063075694 | 270 TABLET in 1 BOTTLE, PLASTIC (43063-756-94) | 270 tablet | 2017-04-24 | 0000-00-00 | No | No | Current |