Package 42708-183-56

Brand: hyoscyamine sulfate tab

Generic: hyoscyamine sulfate
NDC Package Sample

Package Facts

Identity

Package NDC 42708-183-56
Digits Only 4270818356
Product NDC 42708-183
Description

56 TABLET in 1 BOTTLE, PLASTIC (42708-183-56)

Marketing

Marketing Status
Marketed Since 2023-05-26
Brand hyoscyamine sulfate tab
Generic hyoscyamine sulfate
Sample Package Yes

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "46539e99-e8c6-7994-e063-6294a90a0a7c", "openfda": {"unii": ["F2R8V82B84"], "rxcui": ["1047905"], "spl_set_id": ["fc7566e6-c043-fcd4-e053-6294a90a77e5"], "manufacturer_name": ["QPharma, Inc."]}, "finished": true, "packaging": [{"sample": true, "description": "56 TABLET in 1 BOTTLE, PLASTIC (42708-183-56)", "package_ndc": "42708-183-56", "marketing_start_date": "20230526"}], "brand_name": "Hyoscyamine Sulfate TAB", "product_id": "42708-183_46539e99-e8c6-7994-e063-6294a90a0a7c", "dosage_form": "TABLET", "product_ndc": "42708-183", "generic_name": "hyoscyamine sulfate", "labeler_name": "QPharma, 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": "20110519", "listing_expiration_date": "20261231"}