Carbidopa and Levodopa
- Product NDC
- 51407-168
- 11-digit product format
- 514070168
- Labeler code
- 51407
- Product ID
- 51407-168_e5feaf32-88e9-5080-e053-2a95a90a51a0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Carbidopa and Levodopa
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Golden State Medical Supply
- Application
- ANDA073607
- Marketing category
- ANDA
- Marketing start
- 1992-08-28
- 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 |
|---|
| 51407-168-01 | 51407016801 | 100 TABLET in 1 BOTTLE (51407-168-01) | 100 tablet | 2018-07-28 | 0000-00-00 | No | No | Current |
| 51407-168-05 | 51407016805 | 500 TABLET in 1 BOTTLE (51407-168-05) | 500 tablet | 2018-07-28 | 0000-00-00 | No | No | Current |