Gabapentin
- Product NDC
- 0615-8098
- 11-digit product format
- 006158098
- Labeler code
- 0615
- Product ID
- 0615-8098_da90c0b7-6f77-49a8-a895-001c36070a35
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Gabapentin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NCS HealthCare of KY, Inc dba Vangard Labs
- Application
- ANDA077662
- Marketing category
- ANDA
- Marketing start
- 2006-04-01
- Marketing end
- 2021-05-31
- 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
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 0615-8098-05 | 00615809805 | 15 TABLET in 1 BLISTER PACK (0615-8098-05) | 15 tablet | 2017-07-07 | 2021-05-31 | No | No | Current |
| 0615-8098-39 | 00615809839 | 30 TABLET in 1 BLISTER PACK (0615-8098-39) | 30 tablet | 2017-07-07 | 2021-05-31 | No | No | Current |