Propafenone Hydrochloride
- Product NDC
- 63629-2271
- 11-digit product format
- 636292271
- Labeler code
- 63629
- Product ID
- 63629-2271_ae60bd92-3de2-4e30-b46e-681a09fec94f
- 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
- 0000-00-00
- Substance
- PROPAFENONE HYDROCHLORIDE
- Active strength
- 325 mg/1
- Pharmacologic classes
- Antiarrhythmic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 63629-2271-1 | 63629227101 | 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (63629-2271-1) | 2021-03-29 | 0000-00-00 | No | No | Current |