Propafenone Hydrochloride
- Product NDC
- 72162-1751
- 11-digit product format
- 721621751
- Labeler code
- 72162
- Product ID
- 72162-1751_4bc2f877-9021-c8aa-e063-6294a90adc52
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Propafenone Hydrochloride
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA076550
- Marketing category
- ANDA
- Marketing start
- 2015-03-31
- Substance
- PROPAFENONE HYDROCHLORIDE
- Active strength
- 150 mg/1
- Pharmacologic classes
- Antiarrhythmic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 33XCH0HOCD | PROPAFENONE HYDROCHLORIDE | 34183-22-7 | PROPAFENONE HYDROCHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-1751-1 | 72162175101 | 100 TABLET, COATED in 1 BOTTLE (72162-1751-1) | 2023-08-30 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Propafenone Hydrochloride | Bryant Ranch Prepack | 2026-02-26 | HUMAN PRESCRIPTION DRUG LABEL | 101 |