Hyoscyamine
Hyoscyamine Sulfate Extended-Release Tablets, 0.375 mg Rx only
Approved
Approval ID
5bbce8c0-a9c9-45b9-8457-1542bd3d9449
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Apr 11, 2016
Manufacturers
FDA
Wallace Pharmaceuticals Inc.
DUNS: 962531955
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
hyoscyamine sulfate
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code51525-0115
Product Classification
G
Generic Name
hyoscyamine sulfate
Product Specifications
Route of AdministrationORAL
Effective DateApril 11, 2016
FDA Product Classification
INGREDIENTS (1)
HYOSCYAMINE SULFATEActive
Quantity: 0.375 mg in 1 1
Code: F2R8V82B84
Classification: ACTIB