Propafenone Hydrochloride
- Product NDC
- 0603-5450
- 11-digit product format
- 006035450
- Labeler code
- 0603
- Product ID
- 0603-5450_b375fca8-7731-4563-a237-2b066af75310
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Propafenone Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Par Pharmaceutical, Inc.
- Application
- ANDA075938
- Marketing category
- ANDA
- Marketing start
- 2002-10-17
- Marketing end
- 2024-03-31
- Substance
- PROPAFENONE HYDROCHLORIDE
- Active strength
- 300 mg/1
- Pharmacologic classes
- Antiarrhythmic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 0603-5450-21 | 00603545021 | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0603-5450-21) | 2002-10-17 | 0000-00-00 | No | No | Current |