Propafenone Hydrochloride
- Product NDC
- 66993-116
- 11-digit product format
- 669930116
- Labeler code
- 66993
- Product ID
- 66993-116_4f150e81-3780-4968-a9c7-d04d0bebcc52
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- propafenone hydrochloride
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Prasco Laboratories
- Application
- NDA021416
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2014-10-22
- Marketing end
- 2022-02-28
- Substance
- PROPAFENONE HYDROCHLORIDE
- Active strength
- 425 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 |
|---|
| 66993-116-60 | 66993011660 | 60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (66993-116-60) | 2014-10-22 | 2022-02-28 | No | No | Current |