CARBIDOPA AND LEVODOPA
- Product NDC
- 62756-985
- 11-digit product format
- 627560985
- Labeler code
- 62756
- Product ID
- 62756-985_d77ed25a-588d-4d22-855f-f93ba5b4003c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- CARBIDOPA AND LEVODOPA
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Application
- ANDA078536
- Marketing category
- ANDA
- Marketing start
- 2021-08-12
- 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 |
|---|
| 62756-985-01 | 62756098501 | 100 TABLET in 1 BOTTLE (62756-985-01) | 100 tablet | 2021-08-12 | No | No | Historical |
| 62756-985-02 | 62756098502 | 500 TABLET in 1 BOTTLE (62756-985-02) | 500 tablet | 2021-08-12 | No | No | Historical |