CARBIDOPA AND LEVODOPA
- Product NDC
- 63629-2358
- 11-digit product format
- 636292358
- Labeler code
- 63629
- Product ID
- 63629-2358_51be86e2-e8ee-43d0-8b60-0beeacbbbcaa
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- CARBIDOPA AND LEVODOPA
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA078536
- Marketing category
- ANDA
- Marketing start
- 2008-10-28
- Marketing end
- 2023-06-30
- 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
- 0000-00-00
- 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 |
|---|
| 63629-2358-1 | 63629235801 | 100 TABLET in 1 BOTTLE (63629-2358-1) | 100 tablet | 2008-10-28 | 2023-06-30 | No | No | Current |