Carbidopa and Levodopa
- Product NDC
- 60687-836
- 11-digit product format
- 606870836
- Labeler code
- 60687
- Product ID
- 60687-836_437db9b1-5769-5e31-e063-6394a90aa4fd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Carbidopa and Levodopa
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- ANDA074260
- Marketing category
- ANDA
- Marketing start
- 2024-03-16
- Substance
- CARBIDOPA; LEVODOPA
- Active strength
- 25; 250 mg/1; mg/1
- Pharmacologic classes
- Amino Acids, Aromatic [CS], Aromatic Amino Acid [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| MNX7R8C5VO | CARBIDOPA | 38821-49-7 | CARBIDOPA |
| 46627O600J | LEVODOPA | 59-92-7 | LEVODOPA |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 60687-836-01 | 60687083601 | 100 BLISTER PACK in 1 CARTON (60687-836-01) / 1 TABLET in 1 BLISTER PACK (60687-836-11) | 100 blister pack | 2024-03-16 | No | No | Historical |