Carbidopa and Levodopa
- Product NDC
- 70518-3250
- 11-digit product format
- 705183250
- Labeler code
- 70518
- Product ID
- 70518-3250_cf563392-4524-03e7-e053-2995a90adaeb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Carbidopa and Levodopa
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA214092
- Marketing category
- ANDA
- Marketing start
- 2021-10-20
- Marketing end
- 0000-00-00
- Substance
- CARBIDOPA; LEVODOPA
- Active strength
- 25 mg/1; mg/1
- Pharmacologic classes
- Aromatic Amino Acid [EPC],Amino Acids, Aromatic [CS]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-3250-0 | 70518325000 | 30 TABLET in 1 BLISTER PACK (70518-3250-0) | 30 tablet | 2021-10-20 | 0000-00-00 | No | No | Current |