GABAPENTIN
- Product NDC
- 60760-627
- 11-digit product format
- 607600627
- Labeler code
- 60760
- Product ID
- 60760-627_7a8ec319-cd47-4284-e053-2991aa0a7d75
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- GABAPENTIN
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- St. Mary
- Application
- ANDA090705
- Marketing category
- ANDA
- Marketing start
- 2016-11-22
- 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
- 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 |
|---|
| 60760-627-60 | 60760062760 | 60 CAPSULE in 1 BOTTLE, PLASTIC (60760-627-60) | 60 capsule | 2016-11-22 | 0000-00-00 | No | No | Current |