CARBIDOPA AND LEVODOPA
- Product NDC
- 67046-1668
- 11-digit product format
- 670461668
- Labeler code
- 67046
- Product ID
- 67046-1668_500f063b-fab2-993b-e063-6394a90aa366
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Carbidopa and Levodopa
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Coupler LLC
- Application
- ANDA218939
- Marketing category
- ANDA
- Marketing start
- 2026-04-22
- Substance
- CARBIDOPA; LEVODOPA
- Active strength
- 25; 250 mg/1; mg/1
- Pharmacologic classes
- Amino Acids, Aromatic [CS], Aromatic Amino Acid [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- CARBIDOPA AND LEVODOPA
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| CARBIDOPA | 25 mg/1 |
| LEVODOPA | 250 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | MNX7R8C5VO, 46627O600J |
| Rxcui | 197445 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 67046-1668-3 | CARBIDOPA AND LEVODOPA | 30 in 1 BLISTER PACK | TABLET | 30 | | 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 |
|---|
| 67046-1668-3 | 67046166803 | 30 TABLET in 1 BLISTER PACK (67046-1668-3) | 30 tablet | 2026-04-22 | No | No | Historical |