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Hyoscyamine Sulfate SL

Hyoscyamine Sulfate SublingualTablets, USP

Approved
Approval ID

c5049243-5741-4d60-b65e-f3102fa7cc56

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Mar 1, 2009

Manufacturers
FDA

Franklin Pharmaceutical LLC

DUNS: 961561581

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 Code50532-113
Product Classification
G
Generic Name
HYOSCYAMINE SULFATE
Product Specifications
Route of AdministrationORAL
Effective DateMarch 1, 2009
FDA Product Classification

INGREDIENTS (7)

Lactose MonohydrateInactive
Code: EWQ57Q8I5X
Classification: IACT
Starch, CornInactive
Code: O8232NY3SJ
Classification: IACT
MannitolInactive
Code: 3OWL53L36A
Classification: IACT
Stearic AcidInactive
Code: 4ELV7Z65AP
Classification: IACT
FD&C BLUE NO. 1Inactive
Code: H3R47K3TBD
Classification: IACT
Magnesium StearateInactive
Code: 70097M6I30
Classification: IACT
HYOSCYAMINE SULFATEActive
Quantity: 0.125 mg in 1 1
Code: F2R8V82B84
Classification: ACTIB

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Hyoscyamine Sulfate SL - FDA Drug Approval Details