Propafenone Hydrochloride
- Product NDC
- 71335-2780
- 11-digit product format
- 713352780
- Labeler code
- 71335
- Product ID
- 71335-2780_8091654a-d552-41b3-b090-2ae99ef6dee3
- 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
- 2026-12-31
- 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 |
|---|
| 71335-2780-1 | 71335278001 | 30 TABLET, COATED in 1 BOTTLE (71335-2780-1) | 2025-10-13 | No | No | Historical |
| 71335-2780-2 | 71335278002 | 90 TABLET, COATED in 1 BOTTLE (71335-2780-2) | 2025-10-13 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Propafenone Hydrochloride | Bryant Ranch Prepack | 2025-10-13 | HUMAN PRESCRIPTION DRUG LABEL | 1 |