Propafenone Hydrochloride
- Product NDC
- 42291-545
- 11-digit product format
- 422910545
- Labeler code
- 42291
- Product ID
- 42291-545_d221da1f-fd60-4540-8391-73d1615ccf76
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- propafenone hydrochloride
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- AvKARE, Inc.
- Application
- ANDA078540
- Marketing category
- ANDA
- Marketing start
- 2016-01-21
- Marketing end
- 0000-00-00
- Substance
- PROPAFENONE HYDROCHLORIDE
- Active strength
- 225 mg/1
- Pharmacologic classes
- Antiarrhythmic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 42291-545-60 | 42291054560 | 60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (42291-545-60) | 2016-01-21 | 0000-00-00 | No | No | Current |