Carbidopa and Levodopa
- Product NDC
- 0378-5051
- 11-digit product format
- 003785051
- Labeler code
- 0378
- Product ID
- 0378-5051_c9f6ebac-312d-4f8f-b19c-c9f12e97588f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- carbidopa and levodopa
- Dosage form
- TABLET, ORALLY DISINTEGRATING
- Route
- ORAL
- Labeler
- Mylan Pharmaceuticals Inc.
- Application
- ANDA078893
- Marketing category
- ANDA
- Marketing start
- 2008-09-18
- Marketing end
- 0000-00-00
- Substance
- CARBIDOPA; LEVODOPA
- Active strength
- 10 mg/1; mg/1
- Pharmacologic classes
- Aromatic Amino Acid [EPC],Amino Acids, Aromatic [CS]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0378-5051-01 | 00378505101 | 100 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE, PLASTIC (0378-5051-01) | 2008-09-18 | 0000-00-00 | No | No | Current |