CARBIDOPA AND LEVODOPA
- Product NDC
- 68071-2240
- 11-digit product format
- 680712240
- Labeler code
- 68071
- Product ID
- 68071-2240_1d7656b4-b2d1-e4f7-e063-6394a90ab933
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- CARBIDOPA AND LEVODOPA
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA078536
- Marketing category
- ANDA
- Marketing start
- 2008-10-28
- Substance
- CARBIDOPA; LEVODOPA
- Active strength
- 25; 100 mg/1; mg/1
- Pharmacologic classes
- Amino Acids, Aromatic [CS], Aromatic Amino Acid [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- CARBIDOPA AND LEVODOPA
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| CARBIDOPA | 25 mg/1 |
| LEVODOPA | 100 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | MNX7R8C5VO, 46627O600J |
| Rxcui | 197444 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 68071-2240-1 | CARBIDOPA AND LEVODOPA | 100 in 1 BOTTLE | TABLET | 100 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68071-2240 | CARBIDOPA AND LEVODOPA TABLET [NUCARE PHARMACEUTICALS,INC.] | 3 | Current NDC, Legacy NDC, 1 package rows | 20240719_ad2ab0c4-188b-f025-e053-2a95a90a2816.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-2240-1 | 68071224001 | 100 TABLET in 1 BOTTLE (68071-2240-1) | 100 tablet | 2020-08-18 | 0000-00-00 | No | No | Current |