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Hyoscyamine Sulfate - 63629-4838-1 - (Hyoscyamine Sulfate)

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Drug Information of Hyoscyamine Sulfate

Product NDC: 63629-4838
Proprietary Name: Hyoscyamine Sulfate
Non Proprietary Name: Hyoscyamine Sulfate
Active Ingredient(s): .125    mg/1 & nbsp;   Hyoscyamine Sulfate
Administration Route(s): ORAL; SUBLINGUAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Hyoscyamine Sulfate

Product NDC: 63629-4838
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20090921

Package Information of Hyoscyamine Sulfate

Package NDC: 63629-4838-1
Package Description: 20 TABLET in 1 BOTTLE (63629-4838-1)

NDC Information of Hyoscyamine Sulfate

NDC Code 63629-4838-1
Proprietary Name Hyoscyamine Sulfate
Package Description 20 TABLET in 1 BOTTLE (63629-4838-1)
Product NDC 63629-4838
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hyoscyamine Sulfate
Dosage Form Name TABLET
Route Name ORAL; SUBLINGUAL
Start Marketing Date 20090921
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Bryant Ranch Prepack
Substance Name HYOSCYAMINE SULFATE
Strength Number .125
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Hyoscyamine Sulfate


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