Carbidopa and levodopa
- Product NDC
- 0904-7257
- 11-digit product format
- 009047257
- Labeler code
- 0904
- Product ID
- 0904-7257_a6c68d7d-d535-4dcd-a0e2-499ac8884dc6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Carbidopa and levodopa
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Major Pharmaceuticals
- Application
- ANDA074260
- Marketing category
- ANDA
- Marketing start
- 2022-01-18
- Marketing end
- 0000-00-00
- Substance
- CARBIDOPA; LEVODOPA
- Active strength
- 25 mg/1; mg/1
- Pharmacologic classes
- Amino Acids, Aromatic [CS], Aromatic Amino Acid [EPC]
- 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 |
|---|
| 0904-7257-61 | 00904725761 | 100 BLISTER PACK in 1 CARTON (0904-7257-61) > 1 TABLET in 1 BLISTER PACK | 100 blister pack | 2022-01-18 | 0000-00-00 | No | No | Current |