Carbidopa and Levodopa
- Product NDC
- 51862-856
- 11-digit product format
- 518620856
- Labeler code
- 51862
- Product ID
- 51862-856_b2a61d0f-e190-494b-8016-f0d824d9b3dd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Carbidopa and Levodopa
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Mayne Pharma Inc.
- Application
- ANDA073589
- Marketing category
- ANDA
- Marketing start
- 2018-07-16
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51862-856 | CARBIDOPA AND LEVODOPA TABLET [MAYNE PHARMA COMMERCIAL LLC] | 7 | Legacy NDC | 20250402_d92bf9c8-ec59-4a7d-996f-2727d6e6adc5.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 51862-856-01 | 51862085601 | 100 TABLET in 1 BOTTLE (51862-856-01) | 100 tablet | 2018-07-16 | 0000-00-00 | No | No | Current |
| 51862-856-05 | 51862085605 | 500 TABLET in 1 BOTTLE (51862-856-05) | 500 tablet | 2018-07-16 | 0000-00-00 | No | No | Current |
| 51862-856-10 | 51862085610 | 1000 TABLET in 1 BOTTLE (51862-856-10) | 1000 tablet | 2018-07-16 | 0000-00-00 | No | No | Current |