DIGOXIN
- Product NDC
- 70518-0338
- 11-digit product format
- 705180338
- Labeler code
- 70518
- Product ID
- 70518-0338_83d37d5a-ed63-e142-e053-2991aa0ad846
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- DIGOXIN
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- NDA020405
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2017-03-20
- Marketing end
- 0000-00-00
- Substance
- DIGOXIN
- Active strength
- 0 mg/1
- Pharmacologic classes
- Cardiac Glycoside [EPC],Cardiac Glycosides [CS]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record