Carbidopa and Levodopa
- Product NDC
- 65084-108
- 11-digit product format
- 650840108
- Labeler code
- 65084
- Product ID
- 65084-108_ba7724ab-fe79-4f04-e053-2995a90a54ff
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Carbidopa and Levodopa
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- McKesson Corporation dba RX Pak
- Application
- ANDA073589
- Marketing category
- ANDA
- Marketing start
- 2018-07-16
- Marketing end
- 2021-03-31
- 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 65084-108-10 | 65084010810 | 10 BLISTER PACK in 1 BOX (65084-108-10) > 10 TABLET in 1 BLISTER PACK | 10 blister pack | 2019-10-01 | 2021-03-31 | No | No | Current |