Carbidopa and levodopa
- Product NDC
- 42291-465
- 11-digit product format
- 422910465
- Labeler code
- 42291
- Product ID
- 42291-465_ec6b1784-5aad-d816-e053-2a95a90a18c8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Carbidopa and levodopa
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- AvKARE
- Application
- ANDA074260
- Marketing category
- ANDA
- Marketing start
- 2021-04-06
- Marketing end
- 2023-02-28
- Substance
- CARBIDOPA; LEVODOPA
- Active strength
- 10 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
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 42291-465-01 | Carbidopa and levodopa | 100 in 1 BOTTLE | TABLET | 100 | | 4 |
| 42291-465-50 | Carbidopa and levodopa | 500 in 1 BOTTLE | TABLET | 500 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 42291-465 | CARBIDOPA AND LEVODOPA TABLET [AVKARE] | 3 | Legacy NDC, 2 package rows | 20240110_bf52f4bc-a435-4938-e053-2995a90a6774.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 42291-465-01 | 42291046501 | 100 TABLET in 1 BOTTLE (42291-465-01) | 100 tablet | 2021-04-06 | 0000-00-00 | No | No | Current |
| 42291-465-50 | 42291046550 | 500 TABLET in 1 BOTTLE (42291-465-50) | 500 tablet | 2021-04-06 | 0000-00-00 | No | No | Current |