Carbidopa-levodopa
- Product NDC
- 71335-2588
- 11-digit product format
- 713352588
- Labeler code
- 71335
- Product ID
- 71335-2588_c8a94e9a-d796-4af7-ba62-c8a54f3648c2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- carbidopa and levodopa
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA216505
- Marketing category
- ANDA
- Marketing start
- 2022-09-21
- 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-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 |
|---|
| 71335-2588-1 | Carbidopa-levodopa | 90 in 1 BOTTLE | TABLET | 90 | | 1 |
| 71335-2588-2 | Carbidopa-levodopa | 60 in 1 BOTTLE | TABLET | 60 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71335-2588-1 | 71335258801 | 90 TABLET in 1 BOTTLE (71335-2588-1) | 90 tablet | 2025-06-04 | No | No | Current |
| 71335-2588-2 | 71335258802 | 60 TABLET in 1 BOTTLE (71335-2588-2) | 60 tablet | 2025-06-04 | No | No | Current |