Carbidopa and Levodopa
- Product NDC
- 0615-4568
- 11-digit product format
- 006154568
- Labeler code
- 0615
- Product ID
- 0615-4568_5b049995-c25b-40e5-8750-739125ad1b51
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Carbidopa and Levodopa
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- NCS HealthCare of KY, Inc dba Vangard Labs
- Application
- ANDA075091
- Marketing category
- ANDA
- Marketing start
- 2011-10-18
- Marketing end
- 0000-00-00
- Substance
- CARBIDOPA; LEVODOPA
- Active strength
- 50 mg/1; mg/1
- Pharmacologic classes
- Aromatic Amino Acid [EPC],Amino Acids, Aromatic [CS]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#