Carbidopa and Levodopa
- Product NDC
- 0615-8536
- 11-digit product format
- 006158536
- Labeler code
- 0615
- Product ID
- 0615-8536_4bccc4b9-7399-4dd4-9146-c5b2714f299f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Carbidopa and Levodopa
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NCS HealthCare of KY, LLC dba Vangard Labs
- Application
- ANDA073589
- Marketing category
- ANDA
- Marketing start
- 2024-05-01
- 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
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| MNX7R8C5VO | CARBIDOPA | 38821-49-7 | CARBIDOPA |
| 46627O600J | LEVODOPA | 59-92-7 | LEVODOPA |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 0615-8536-05 | 00615853605 | 15 TABLET in 1 BLISTER PACK (0615-8536-05) | 15 tablet | 2024-09-10 | No | No | Historical |
| 0615-8536-28 | 00615853628 | 28 TABLET in 1 BLISTER PACK (0615-8536-28) | 28 tablet | 2024-09-10 | No | No | Historical |
| 0615-8536-39 | 00615853639 | 30 TABLET in 1 BLISTER PACK (0615-8536-39) | 30 tablet | 2024-09-10 | No | No | Historical |