Gabapentin
- Product NDC
- 43063-664
- 11-digit product format
- 430630664
- Labeler code
- 43063
- Product ID
- 43063-664_d60bc9bc-faac-2ff6-e053-2995a90abf3c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Gabapentin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA078787
- Marketing category
- ANDA
- Marketing start
- 2008-01-31
- Marketing end
- 0000-00-00
- Substance
- GABAPENTIN
- Active strength
- 100 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 43063-664-30 | 43063066430 | 30 CAPSULE in 1 BOTTLE, PLASTIC (43063-664-30) | 30 capsule | 2008-01-31 | 0000-00-00 | No | No | Current |
| 43063-664-60 | 43063066460 | 60 CAPSULE in 1 BOTTLE, PLASTIC (43063-664-60) | 60 capsule | 2008-01-31 | 0000-00-00 | No | No | Current |
| 43063-664-90 | 43063066490 | 90 CAPSULE in 1 BOTTLE, PLASTIC (43063-664-90) | 90 capsule | 2008-01-31 | 0000-00-00 | No | No | Current |