Carbidopa and Levodopa
- Product NDC
- 60687-661
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Carbidopa and Levodopa
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- ANDA074260
- Marketing category
- ANDA
- Substance
- CARBIDOPA; LEVODOPA
- Current FDA listing
- Yes
Related Records
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|---|---|---|---|---|
| 60687-661-01 | 100 BLISTER PACK in 1 CARTON (60687-661-01) / 1 TABLET in 1 BLISTER PACK (60687-661-11) | 2022-05-27 | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|---|---|---|---|
| Carbidopa and Levodopa Tablets, USP 8466101/0224(F) Rx only | American Health Packaging | 2025-11-13 | HUMAN PRESCRIPTION DRUG LABEL | 4 |
| Carbidopa and Levodopa Tablets, USP 8466101/0224 Rx only | American Health Packaging | 2024-03-14 | HUMAN PRESCRIPTION DRUG LABEL | 3 |