hyoscyamine sulfate odt

Generic: hyoscyamine sulfate

Labeler: westminster pharmaceuticals, llc
NDC Directory HUMAN PRESCRIPTION DRUG UNAPPROVED DRUG OTHER Inactive Finished

Drug Facts

Product Profile

Brand Name hyoscyamine sulfate odt
Generic Name hyoscyamine sulfate
Labeler westminster pharmaceuticals, llc
Dosage Form TABLET, ORALLY DISINTEGRATING
Routes
ORAL
Active Ingredients

hyoscyamine sulfate .125 mg/1

Manufacturer
Westminster Pharmaceuticals, LLC

Identifiers & Regulatory

Product NDC 69367-679
Product ID 69367-679_d40f28c0-8358-4b25-a957-568e01125dfe
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category UNAPPROVED DRUG OTHER
Listing Expiration 2026-12-31
Marketing Start 2025-04-02

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 69367679
Hyphenated Format 69367-679

Supplemental Identifiers

RxCUI
1046985
UPC
0369367679015
UNII
F2R8V82B84

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name hyoscyamine sulfate odt (source: ndc)
Generic Name hyoscyamine sulfate (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • .125 mg/1
source: ndc
Packaging
  • 100 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (69367-679-01)
source: ndc

Packages (1)

69367-679-01 100 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (69367-679-01)

Ingredients (1)

hyoscyamine sulfate (.125 mg/1)

Linked Drug Pages (1)

Hyoscyamine Sulfate ODT ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "d40f28c0-8358-4b25-a957-568e01125dfe", "openfda": {"upc": ["0369367679015"], "unii": ["F2R8V82B84"], "rxcui": ["1046985"], "spl_set_id": ["9429898d-301f-4ebc-8b1d-60595f76f1e3"], "manufacturer_name": ["Westminster Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (69367-679-01)", "package_ndc": "69367-679-01", "marketing_start_date": "20250402"}], "brand_name": "Hyoscyamine Sulfate ODT", "product_id": "69367-679_d40f28c0-8358-4b25-a957-568e01125dfe", "dosage_form": "TABLET, ORALLY DISINTEGRATING", "product_ndc": "69367-679", "generic_name": "Hyoscyamine Sulfate", "labeler_name": "Westminster Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hyoscyamine Sulfate", "brand_name_suffix": "ODT", "active_ingredients": [{"name": "HYOSCYAMINE SULFATE", "strength": ".125 mg/1"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20250402", "listing_expiration_date": "20261231"}