Carbidopa and levodopa
- Product NDC
- 50090-3419
- 11-digit product format
- 500903419
- Labeler code
- 50090
- Product ID
- 50090-3419_b23e8203-25e4-4dba-8445-387302d76a33
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Carbidopa and levodopa
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA074260
- Marketing category
- ANDA
- Marketing start
- 1993-09-01
- 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 |
|---|
| 50090-3419-0 | 50090341900 | 30 TABLET in 1 BOTTLE (50090-3419-0) | 30 tablet | 2019-10-15 | 0000-00-00 | No | No | Current |
| 50090-3419-1 | 50090341901 | 90 TABLET in 1 BOTTLE (50090-3419-1) | 90 tablet | 2018-03-26 | 0000-00-00 | No | No | Current |
| 50090-3419-2 | 50090341902 | 270 TABLET in 1 BOTTLE (50090-3419-2) | 270 tablet | 2022-03-10 | 0000-00-00 | No | No | Current |
| 50090-3419-3 | 50090341903 | 300 TABLET in 1 BOTTLE (50090-3419-3) | 300 tablet | 2022-03-10 | 0000-00-00 | No | No | Current |