Gabapentin
- Product NDC
- 0615-1376
- 11-digit product format
- 006151376
- Labeler code
- 0615
- Product ID
- 0615-1376_d8df25f8-fbd2-41e4-b5b2-a4b10ddd67b2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Gabapentin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- NCS HealthCare of KY, Inc dba Vangard Labs
- Application
- ANDA075350
- Marketing category
- ANDA
- Marketing start
- 2003-09-12
- 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
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#