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NDC 59651-0257-33 PROPAFENONE HYDROCHLORIDE 225 mg/1 Details
PROPAFENONE HYDROCHLORIDE 225 mg/1
PROPAFENONE HYDROCHLORIDE is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Aurobindo Pharma Limited. The primary component is PROPAFENONE HYDROCHLORIDE.
MedlinePlus Drug Summary
Propafenone is used to treat arrhythmia (irregular heartbeat) and to maintain a normal heart rate. Propafenone is in a class of medications called antiarrhythmics. It works by acting on the heart muscle to improve the heart's rhythm.
Related Packages: 59651-0257-33Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Propafenone
Product Information
| NDC | 59651-0257 |
|---|---|
| Product ID | 59651-257_b59b252f-8b73-4f72-8d01-4d2076c18fa6 |
| Associated GPIs | 35300050000325 |
| GCN Sequence Number | 019751 |
| GCN Sequence Number Description | propafenone HCl TABLET 225 MG ORAL |
| HIC3 | A2A |
| HIC3 Description | ANTIARRHYTHMICS |
| GCN | 12433 |
| HICL Sequence Number | 004833 |
| HICL Sequence Number Description | PROPAFENONE HCL |
| Brand/Generic | Generic |
| Proprietary Name | PROPAFENONE HYDROCHLORIDE |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | PROPAFENONE HYDROCHLORIDE |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | TABLET, FILM COATED |
| Route | ORAL |
| Active Ingredient Strength | 225 |
| Active Ingredient Units | mg/1 |
| Substance Name | PROPAFENONE HYDROCHLORIDE |
| Labeler Name | Aurobindo Pharma Limited |
| Pharmaceutical Class | Antiarrhythmic [EPC] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA202445 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 59651-0257-33 (59651025733)
| NDC Package Code | 59651-257-33 |
|---|---|
| Billing NDC | 59651025733 |
| Package | 300 TABLET, FILM COATED in 1 BOTTLE (59651-257-33) |
| Marketing Start Date | 2019-10-25 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |