Gabapentin
- Product NDC
- 80425-0034
- 11-digit product format
- 804250034
- Labeler code
- 80425
- Product ID
- 80425-0034_cfe9d1e8-5e8d-6299-e053-2a95a90a9ecd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Gabapentin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Advanced Rx Pharmacy of Tennessee, LLC
- Application
- ANDA204989
- Marketing category
- ANDA
- Marketing start
- 2016-09-30
- Marketing end
- 0000-00-00
- Substance
- GABAPENTIN
- Active strength
- 300 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 |
|---|
| 80425-0034-1 | 80425003401 | 30 CAPSULE in 1 BOTTLE (80425-0034-1) | 30 capsule | 2016-09-30 | 0000-00-00 | No | No | Current |
| 80425-0034-2 | 80425003402 | 60 CAPSULE in 1 BOTTLE (80425-0034-2) | 60 capsule | 2016-09-30 | 0000-00-00 | No | No | Current |
| 80425-0034-3 | 80425003403 | 90 CAPSULE in 1 BOTTLE (80425-0034-3) | 90 capsule | 2016-09-30 | 0000-00-00 | No | No | Current |