Gabapentin
- Product NDC
- 60760-123
- 11-digit product format
- 607600123
- Labeler code
- 60760
- Product ID
- 60760-123_ac26196f-5b8d-a3f9-e053-2a95a90a4c96
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Gabapentin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- St. Mary's Medical Park Pharmacy
- Application
- ANDA077662
- Marketing category
- ANDA
- Marketing start
- 2006-04-01
- 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
- 2021-12-31
- 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 |
|---|
| 60760-123-30 | 60760012330 | 30 TABLET in 1 BOTTLE, PLASTIC (60760-123-30) | 30 tablet | 2017-11-28 | 0000-00-00 | No | No | Current |
| 60760-123-60 | 60760012360 | 60 TABLET in 1 BOTTLE, PLASTIC (60760-123-60) | 60 tablet | 2017-11-28 | 0000-00-00 | No | No | Current |
| 60760-123-90 | 60760012390 | 90 TABLET in 1 BOTTLE, PLASTIC (60760-123-90) | 90 tablet | 2017-11-28 | 0000-00-00 | No | No | Current |