Gabapentin
- Product NDC
- 63739-984
- 11-digit product format
- 637390984
- Labeler code
- 63739
- Product ID
- 63739-984_ef6893b2-11f7-a873-e053-2995a90a1f56
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Gabapentin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Mckesson Corporation DBA SKY Packaginng
- Application
- ANDA078428
- Marketing category
- ANDA
- Marketing start
- 2009-11-24
- Marketing end
- 0000-00-00
- Substance
- GABAPENTIN
- Active strength
- 400 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63739-984-10 | 63739098410 | 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-984-10) > 10 CAPSULE in 1 BLISTER PACK | 10 blister pack | 2009-11-24 | 0000-00-00 | No | No | Current |