Gabapentin
- Product NDC
- 55700-686
- 11-digit product format
- 557000686
- Labeler code
- 55700
- Product ID
- 55700-686_503fffe2-3a5a-4a34-8728-e0cc9f5b6c8b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Gabapentin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA205101
- Marketing category
- ANDA
- Marketing start
- 2018-09-21
- Marketing end
- 0000-00-00
- 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
- 2022-12-31
- 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 |
|---|
| 55700-686-30 | 55700068630 | 30 TABLET in 1 BOTTLE (55700-686-30) | 30 tablet | 2018-09-21 | 0000-00-00 | No | No | Current |
| 55700-686-60 | 55700068660 | 60 TABLET in 1 BOTTLE (55700-686-60) | 60 tablet | 2018-09-21 | 0000-00-00 | No | No | Current |