GABAPENTIN
- Product NDC
- 61919-677
- 11-digit product format
- 619190677
- Labeler code
- 61919
- Product ID
- 61919-677_8643d513-86d0-cea3-e053-2991aa0a0ddd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- GABAPENTIN
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- DIRECTRX
- Application
- ANDA077662
- Marketing category
- ANDA
- Marketing start
- 2019-04-11
- 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
- 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 |
|---|
| 61919-677-30 | 61919067730 | 30 TABLET in 1 BOTTLE (61919-677-30) | 30 tablet | 2019-04-11 | 0000-00-00 | No | No | Current |