Carbidopa
- Product NDC
- 51407-314
- 11-digit product format
- 514070314
- Labeler code
- 51407
- Product ID
- 51407-314_a0fbd3e8-7e83-e808-e053-2a95a90a5336
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Carbidopa
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Golden State Medical Supply
- Application
- ANDA204763
- Marketing category
- ANDA
- Marketing start
- 2017-10-20
- Marketing end
- 0000-00-00
- Substance
- CARBIDOPA
- Active strength
- 25 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 51407-314-01 | 51407031401 | 100 TABLET in 1 BOTTLE (51407-314-01) | 100 tablet | 2020-01-30 | 0000-00-00 | No | No | Current |