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Hyoscyamine Sulfate - 50532-115-10 - (HYOSCYAMINE SULFATE)

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Drug Information of Hyoscyamine Sulfate

Product NDC: 50532-115
Proprietary Name: Hyoscyamine Sulfate
Non Proprietary Name: HYOSCYAMINE SULFATE
Active Ingredient(s): .375    mg/1 & nbsp;   HYOSCYAMINE SULFATE
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Hyoscyamine Sulfate

Product NDC: 50532-115
Labeler Name: Franklin Pharmaceutical LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20100501

Package Information of Hyoscyamine Sulfate

Package NDC: 50532-115-10
Package Description: 100 TABLET in 1 BOTTLE, PLASTIC (50532-115-10)

NDC Information of Hyoscyamine Sulfate

NDC Code 50532-115-10
Proprietary Name Hyoscyamine Sulfate
Package Description 100 TABLET in 1 BOTTLE, PLASTIC (50532-115-10)
Product NDC 50532-115
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name HYOSCYAMINE SULFATE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100501
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Franklin Pharmaceutical LLC
Substance Name HYOSCYAMINE SULFATE
Strength Number .375
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Hyoscyamine Sulfate


General Information