Digoxin
- Product NDC
- 70954-154
- 11-digit product format
- 709540154
- Labeler code
- 70954
- Product ID
- 70954-154_748fbf89-14d9-4254-9465-5b24a0aa4d45
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Digoxin
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Novitium Pharma LLC
- Application
- ANDA213000
- Marketing category
- ANDA
- Marketing start
- 2019-10-04
- Marketing end
- 0000-00-00
- Substance
- DIGOXIN
- Active strength
- 0 mg/mL
- 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