Gabapentin
- Product NDC
- 60760-557
- 11-digit product format
- 607600557
- Labeler code
- 60760
- Product ID
- 60760-557_7a8ef282-d7a7-0ae9-e053-2991aa0ad812
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Gabapentin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- St. Mary's Medical Park Pharmacy
- Application
- ANDA075350
- Marketing category
- ANDA
- Marketing start
- 2017-12-15
- Marketing end
- 0000-00-00
- Substance
- GABAPENTIN
- Active strength
- 400 mg/1
- Pharmacologic classes
- Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 60760-557-90 | 60760055790 | 90 CAPSULE in 1 BOTTLE, PLASTIC (60760-557-90) | 90 capsule | 2017-12-15 | 0000-00-00 | No | No | Current |