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NDC 42806-0513-01 QUINIDINE SULFATE 200 mg/1 Details
QUINIDINE SULFATE 200 mg/1
QUINIDINE SULFATE is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by EPIC PHARMA, LLC. The primary component is QUINIDINE SULFATE.
MedlinePlus Drug Summary
Quinidine is used to treat certain types of irregular heartbeats. Quinidine is in a class of medications called antiarrhythmic medications. It works by making your heart more resistant to abnormal activity.
Related Packages: 42806-0513-01Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Quinidine
Product Information
NDC | 42806-0513 |
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Product ID | 42806-513_80df716e-b0d6-4b0f-b0f4-879874d7ed05 |
Associated GPIs | 35100030300310 |
GCN Sequence Number | 000222 |
GCN Sequence Number Description | quinidine sulfate TABLET 200 MG ORAL |
HIC3 | A2A |
HIC3 Description | ANTIARRHYTHMICS |
GCN | 01053 |
HICL Sequence Number | 000075 |
HICL Sequence Number Description | QUINIDINE SULFATE |
Brand/Generic | Generic |
Proprietary Name | QUINIDINE SULFATE |
Proprietary Name Suffix | n/a |
Non-Proprietary Name | quinidine sulfate tablet |
Product Type | HUMAN PRESCRIPTION DRUG |
Dosage Form | TABLET |
Route | ORAL |
Active Ingredient Strength | 200 |
Active Ingredient Units | mg/1 |
Substance Name | QUINIDINE SULFATE |
Labeler Name | EPIC PHARMA, LLC |
Pharmaceutical Class | Antiarrhythmic [EPC], Cytochrome P450 2D6 Inhibitor [EPC], Cytochrome P450 2D6 Inhibitors [MoA] |
DEA Schedule | n/a |
Marketing Category | ANDA |
Application Number | ANDA088072 |
Listing Certified Through | 2024-12-31 |
Package
NDC 42806-0513-01 (42806051301)
NDC Package Code | 42806-513-01 |
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Billing NDC | 42806051301 |
Package | 100 TABLET in 1 BOTTLE (42806-513-01) |
Marketing Start Date | 2021-12-15 |
NDC Exclude Flag | N |
Pricing Information | N/A |