Carbidopa
- Product NDC
- 63629-1932
- 11-digit product format
- 636291932
- Labeler code
- 63629
- Product ID
- 63629-1932_fbdbbc19-8209-43f1-b8d8-c814b993f12a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Carbidopa
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA203261
- Marketing category
- ANDA
- Marketing start
- 2014-03-10
- Marketing end
- 0000-00-00
- Substance
- CARBIDOPA
- Active strength
- 25 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-1932-1 | 63629193201 | 100 TABLET in 1 BOTTLE (63629-1932-1) | 100 tablet | 2022-02-08 | 0000-00-00 | No | No | Current |