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Hyoscyamine Sulfate Extended-Release - 43199-014-01 - (Hyoscyamine Sulfate Extended-Release)

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Drug Information of Hyoscyamine Sulfate Extended-Release

Product NDC: 43199-014
Proprietary Name: Hyoscyamine Sulfate Extended-Release
Non Proprietary Name: Hyoscyamine Sulfate Extended-Release
Active Ingredient(s): .375    mg/1 & nbsp;   Hyoscyamine Sulfate Extended-Release
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Hyoscyamine Sulfate Extended-Release

Product NDC: 43199-014
Labeler Name: County Line Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20100103

Package Information of Hyoscyamine Sulfate Extended-Release

Package NDC: 43199-014-01
Package Description: 100 TABLET in 1 BOTTLE (43199-014-01)

NDC Information of Hyoscyamine Sulfate Extended-Release

NDC Code 43199-014-01
Proprietary Name Hyoscyamine Sulfate Extended-Release
Package Description 100 TABLET in 1 BOTTLE (43199-014-01)
Product NDC 43199-014
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hyoscyamine Sulfate Extended-Release
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100103
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name County Line Pharmaceuticals, LLC
Substance Name HYOSCYAMINE SULFATE
Strength Number .375
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Hyoscyamine Sulfate Extended-Release


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