Carbidopa and Levodopa
- Product NDC
- 50090-6725
- 11-digit product format
- 500906725
- Labeler code
- 50090
- Product ID
- 50090-6725_6c8edbd2-d24c-46ba-80bc-86291ddfb1ba
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Carbidopa and Levodopa
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA214092
- Marketing category
- ANDA
- Marketing start
- 2021-05-07
- Substance
- CARBIDOPA; LEVODOPA
- Active strength
- 25; 100 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 |
|---|
| 50090-6725-0 | 50090672500 | 90 TABLET in 1 BOTTLE (50090-6725-0) | 90 tablet | 2023-10-06 | No | No | Historical |