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NDC 72789-0138-01 Sotalol Hydrochloride 120 mg/1 Details
Sotalol Hydrochloride 120 mg/1
Sotalol Hydrochloride is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by PD-Rx Pharmaceuticals, Inc.. The primary component is SOTALOL HYDROCHLORIDE.
MedlinePlus Drug Summary
Sotalol is used to treat irregular heartbeats. Sotalol is in a class of medications called antiarrhythmics. It works by acting on the heart muscle to improve the heart's rhythm.
Related Packages: 72789-0138-01Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Sotalol
Product Information
NDC | 72789-0138 |
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Product ID | 72789-138_0632abb2-518b-7c34-e063-6394a90a2318 |
Associated GPIs | 33100045100315 |
GCN Sequence Number | 024097 |
GCN Sequence Number Description | sotalol HCl TABLET 120 MG ORAL |
HIC3 | J7C |
HIC3 Description | BETA-ADRENERGIC BLOCKING AGENTS |
GCN | 39516 |
HICL Sequence Number | 004791 |
HICL Sequence Number Description | SOTALOL HCL |
Brand/Generic | Generic |
Proprietary Name | Sotalol Hydrochloride |
Proprietary Name Suffix | n/a |
Non-Proprietary Name | Sotalol Hydrochloride |
Product Type | HUMAN PRESCRIPTION DRUG |
Dosage Form | TABLET |
Route | ORAL |
Active Ingredient Strength | 120 |
Active Ingredient Units | mg/1 |
Substance Name | SOTALOL HYDROCHLORIDE |
Labeler Name | PD-Rx Pharmaceuticals, Inc. |
Pharmaceutical Class | Adrenergic beta-Antagonists [MoA], Antiarrhythmic [EPC], Cardiac Rhythm Alteration [PE] |
DEA Schedule | n/a |
Marketing Category | ANDA |
Application Number | ANDA075563 |
Listing Certified Through | 2024-12-31 |
Package
NDC 72789-0138-01 (72789013801)
NDC Package Code | 72789-138-01 |
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Billing NDC | 72789013801 |
Package | 100 TABLET in 1 BOTTLE, PLASTIC (72789-138-01) |
Marketing Start Date | 2020-11-06 |
NDC Exclude Flag | N |
Pricing Information | N/A |