CARBIDOPA AND LEVODOPA
- Product NDC
- 66267-649
- 11-digit product format
- 662670649
- Labeler code
- 66267
- Product ID
- 66267-649_9cbdbe41-12a2-6938-e053-2a95a90ae941
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- CARBIDOPA AND LEVODOPA
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- Application
- ANDA078536
- Marketing category
- ANDA
- Marketing start
- 2008-10-28
- Marketing end
- 0000-00-00
- Substance
- CARBIDOPA; LEVODOPA
- Active strength
- 25 mg/1; mg/1
- Pharmacologic classes
- Aromatic Amino Acid [EPC],Amino Acids, Aromatic [CS]
- 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 |
|---|
| 66267-649-90 | 66267064990 | 90 TABLET in 1 BOTTLE (66267-649-90) | 90 tablet | 2016-12-28 | 0000-00-00 | No | No | Current |