hyoscyamine sulfate tab

Generic: hyoscyamine sulfate

Labeler: remedyrepack inc.
NDC Directory HUMAN PRESCRIPTION DRUG UNAPPROVED DRUG OTHER Inactive Finished

Drug Facts

Product Profile

Brand Name hyoscyamine sulfate tab
Generic Name hyoscyamine sulfate
Labeler remedyrepack inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

hyoscyamine sulfate .125 mg/1

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-3847
Product ID 70518-3847_3f8bc3b1-e61e-9f63-e063-6294a90a021a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category UNAPPROVED DRUG OTHER
Listing Expiration 2026-12-31
Marketing Start 2023-08-31

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 705183847
Hyphenated Format 70518-3847

Supplemental Identifiers

RxCUI
1047905
UNII
F2R8V82B84

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 tab (source: ndc)
Generic Name hyoscyamine sulfate (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • .125 mg/1
source: ndc
Packaging
  • 180 TABLET in 1 BOTTLE, PLASTIC (70518-3847-1)
source: ndc

Packages (1)

70518-3847-1 180 TABLET in 1 BOTTLE, PLASTIC (70518-3847-1)

Ingredients (1)

hyoscyamine sulfate (.125 mg/1)

Linked Drug Pages (1)

Hyoscyamine Sulfate TAB ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3f8bc3b1-e61e-9f63-e063-6294a90a021a", "openfda": {"unii": ["F2R8V82B84"], "rxcui": ["1047905"], "spl_set_id": ["c1c89510-6381-466f-be1a-6b104a335b56"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "180 TABLET in 1 BOTTLE, PLASTIC (70518-3847-1)", "package_ndc": "70518-3847-1", "marketing_start_date": "20240627"}], "brand_name": "Hyoscyamine Sulfate TAB", "product_id": "70518-3847_3f8bc3b1-e61e-9f63-e063-6294a90a021a", "dosage_form": "TABLET", "product_ndc": "70518-3847", "generic_name": "hyoscyamine sulfate", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hyoscyamine Sulfate TAB", "active_ingredients": [{"name": "HYOSCYAMINE SULFATE", "strength": ".125 mg/1"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20230831", "listing_expiration_date": "20261231"}