Hyoscyamine
Hyoscyamine Sulfate Extended-Release Tablets, 0.375 mg Rx only (Packaged by Pharma Packaging Solutions, LLC dba Tjoapack LLC)
Approved
Approval ID
01f97804-a6cb-ce6d-e063-6394a90ae220
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Aug 2, 2023
Manufacturers
FDA
Pharma Packaging Solutions, LLC dba Tjopack LLC
DUNS: 928861723
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 Code75929-057
Product Classification
G
Generic Name
hyoscyamine sulfate
Product Specifications
Route of AdministrationORAL
Effective DateAugust 2, 2023
FDA Product Classification
INGREDIENTS (1)
HYOSCYAMINE SULFATEActive
Quantity: 0.375 mg in 1 1
Code: F2R8V82B84
Classification: ACTIB