Gabapentin
- Product NDC
- 63629-8059
- 11-digit product format
- 636298059
- Labeler code
- 63629
- Product ID
- 63629-8059_5d08da0c-0770-48d9-9385-314da08c354a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Gabapentin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA206943
- Marketing category
- ANDA
- Marketing start
- 2018-05-14
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 63629-8059-1 | 63629805901 | 90 CAPSULE in 1 BOTTLE (63629-8059-1) | 90 capsule | 2019-07-25 | 0000-00-00 | No | No | Current |
| 63629-8059-2 | 63629805902 | 30 CAPSULE in 1 BOTTLE (63629-8059-2) | 30 capsule | 2019-07-25 | 0000-00-00 | No | No | Current |