Propafenone HCl
- Product NDC
- 63739-510
- 11-digit product format
- 637390510
- Labeler code
- 63739
- Product ID
- 63739-510_36343a60-3d14-4748-b11f-379eec917b8c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Propafenone hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- McKesson Corporation dba SKY Packaging
- Application
- ANDA075203
- Marketing category
- ANDA
- Marketing start
- 2000-10-24
- Marketing end
- 0000-00-00
- Substance
- PROPAFENONE HYDROCHLORIDE
- Active strength
- 225 mg/1
- Pharmacologic classes
- Antiarrhythmic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#