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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Propafenone Hydrochloride
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| PROPAFENONE HYDROCHLORIDE | 150 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 33XCH0HOCD |
| Rxcui | 861424 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 71335-2780-1 | Propafenone Hydrochloride | 30 in 1 BOTTLE | TABLET, COATED | 30 | | 1 |
| 71335-2780-2 | Propafenone Hydrochloride | 90 in 1 BOTTLE | TABLET, COATED | 90 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| 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 | Current |
| 71335-2780-2 | 71335278002 | 90 TABLET, COATED in 1 BOTTLE (71335-2780-2) | 2025-10-13 | No | No | Current |