PROPAFENONE HYDROCHLORIDE
- Product NDC
- 50090-2949
- 11-digit product format
- 500902949
- Labeler code
- 50090
- Product ID
- 50090-2949_9c10c28a-2c49-42d4-936e-bbb9e6952c2c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- propafenone hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA075998
- Marketing category
- ANDA
- Marketing start
- 2001-11-29
- Marketing end
- 0000-00-00
- Substance
- PROPAFENONE HYDROCHLORIDE
- Active strength
- 225 mg/1
- Pharmacologic classes
- Antiarrhythmic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record