Carbidopa and Levodopa
- Product NDC
- 65084-107
- 11-digit product format
- 650840107
- Labeler code
- 65084
- Product ID
- 65084-107_6ed569a2-db14-410a-bb40-4fc49bf66d9f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Carbidopa and Levodopa
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- McKesson Corporation dba RX Pak
- Application
- ANDA073618
- Marketing category
- ANDA
- Marketing start
- 2018-07-16
- Marketing end
- 0000-00-00
- Substance
- CARBIDOPA; LEVODOPA
- Active strength
- 10 mg/1; mg/1
- Pharmacologic classes
- Aromatic Amino Acid [EPC],Amino Acids, Aromatic [CS]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record