Carbidopa and levodopa
- Product NDC
- 0615-8068
- 11-digit product format
- 006158068
- Labeler code
- 0615
- Product ID
- 0615-8068_571e4338-70da-4e3b-88df-5ffeccba1140
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Carbidopa and levodopa
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NCS HealthCare of KY, Inc dba Vangard Labs
- Application
- ANDA074260
- Marketing category
- ANDA
- Marketing start
- 2016-07-18
- Marketing end
- 2022-02-28
- Substance
- CARBIDOPA; LEVODOPA
- Active strength
- 25 mg/1; mg/1
- Pharmacologic classes
- Aromatic Amino Acid [EPC],Amino Acids, Aromatic [CS]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0615-8068-39 | 00615806839 | 30 TABLET in 1 BLISTER PACK (0615-8068-39) | 30 tablet | 2016-10-05 | 2022-02-28 | No | No | Current |