PROPAFENONE HYDROCHLORIDE
- Product NDC
- 60687-930
- 11-digit product format
- 606870930
- Labeler code
- 60687
- Product ID
- 60687-930_41b16e34-8b2c-19d5-e063-6394a90a8d7e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PROPAFENONE HYDROCHLORIDE
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- ANDA075938
- Marketing category
- ANDA
- Marketing start
- 2025-10-21
- 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 |
|---|
| 60687-930-01 | PROPAFENONE HYDROCHLORIDE | 100 in 1 CARTON | TABLET, FILM COATED | 100 | | 2 |
| 60687-930-11 | PROPAFENONE HYDROCHLORIDE | 1 in 1 BLISTER PACK | TABLET, FILM COATED | 1 | | 2 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 60687-930-01 | 60687093001 | 100 BLISTER PACK in 1 CARTON (60687-930-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-930-11) | 100 blister pack | 2025-10-21 | No | No | Historical |
| 60687-930-11 | 60687093011 | 1 in 1 BLISTER PACK | | | | | Historical |