Gabapentin
- Product NDC
- 60760-173
- 11-digit product format
- 607600173
- Labeler code
- 60760
- Product ID
- 60760-173_b580aadd-1b96-1b2c-e053-2995a90af228
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Gabapentin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- St. Mary
- Application
- ANDA077662
- Marketing category
- ANDA
- Marketing start
- 2015-08-09
- 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
- 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 |
|---|
| 60760-173-90 | 60760017390 | 90 TABLET in 1 BOTTLE, PLASTIC (60760-173-90) | 90 tablet | 2015-08-09 | 0000-00-00 | No | No | Current |
| 60760-173-92 | 60760017392 | 120 TABLET in 1 BOTTLE, PLASTIC (60760-173-92) | 120 tablet | 2015-09-01 | 0000-00-00 | No | No | Current |