Propafenone Hydrochloride
- Product NDC
- 63629-2269
- 11-digit product format
- 636292269
- Labeler code
- 63629
- Product ID
- 63629-2269_8d9da187-2d87-4b72-a675-a67baac63d3e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- propafenone hydrochloride
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA078540
- Marketing category
- ANDA
- Marketing start
- 2011-01-03
- Marketing end
- 2024-09-30
- Substance
- PROPAFENONE HYDROCHLORIDE
- Active strength
- 225 mg/1
- Pharmacologic classes
- Antiarrhythmic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-2269-1 | 63629226901 | 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (63629-2269-1) | 2021-03-29 | 0000-00-00 | No | No | Current |