Gabapentin
- Product NDC
- 68084-802
- 11-digit product format
- 680840802
- Labeler code
- 68084
- Product ID
- 68084-802_a2cda367-14f7-b2ff-e053-2995a90a1f34
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Gabapentin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- ANDA078926
- Marketing category
- ANDA
- Marketing start
- 2014-08-27
- Marketing end
- 2021-04-30
- 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
- 0000-00-00
- 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 |
|---|
| 68084-802-01 | 68084080201 | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-802-01) > 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-802-11) | 100 blister pack | 2014-08-27 | 2021-04-30 | No | No | Current |