PROPAFENONE HYDROCHLORIDE
- Product NDC
- 52536-735
- 11-digit product format
- 525360735
- Labeler code
- 52536
- Product ID
- 52536-735_5f7e4969-d2c4-4871-863b-34f2585a3cda
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PROPAFENONE HYDROCHLORIDE
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Wilshire Pharmaceuticals
- Application
- ANDA205956
- Marketing category
- ANDA
- Marketing start
- 2019-03-21
- Marketing end
- 0000-00-00
- Substance
- PROPAFENONE HYDROCHLORIDE
- Active strength
- 425 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#