Sotalol Hydrochloride
- Product NDC
- 0603-5772
- 11-digit product format
- 006035772
- Labeler code
- 0603
- Product ID
- 0603-5772_2398995d-e533-4306-a436-eb87ff0f064f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sotalol Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Par Pharmaceutical
- Application
- ANDA075563
- Marketing category
- ANDA
- Marketing start
- 2003-11-07
- Marketing end
- 2019-03-31
- Substance
- SOTALOL HYDROCH
- Active strength
- 240 mg/1
- Pharmacologic classes
- Antiarrhythmic
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record