GABAPENTIN
- Product NDC
- 58657-623
- 11-digit product format
- 586570623
- Labeler code
- 58657
- Product ID
- 58657-623_9d53192b-21d5-4cb8-e053-2995a90a29a5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- GABAPENTIN
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Method Pharmaceuticals, LLC
- Application
- ANDA205101
- Marketing category
- ANDA
- Marketing start
- 2016-11-20
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 58657-623-01 | 58657062301 | 100 TABLET in 1 BOTTLE (58657-623-01) | 100 tablet | 2016-11-20 | 0000-00-00 | No | No | Current |
| 58657-623-50 | 58657062350 | 500 TABLET in 1 BOTTLE (58657-623-50) | 500 tablet | 2016-11-20 | 0000-00-00 | No | No | Current |