heartburn relief
Generic: famotidine
Labeler: shield pharmaceuticals corpDrug Facts
Product Profile
Brand Name
heartburn relief
Generic Name
famotidine
Labeler
shield pharmaceuticals corp
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
famotidine 10 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
83059-0005
Product ID
83059-0005_458b9ea6-72d7-b5af-e063-6294a90a4430
Product Type
HUMAN OTC DRUG
Marketing Category
ANDA
Application Number
ANDA215822
Listing Expiration
2026-12-31
Marketing Start
2024-01-16
Pharmacologic Class
Established (EPC)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
830590005
Hyphenated Format
83059-0005
Supplemental Identifiers
RxCUI
UNII
NUI
Packaging Origin
Original Packager
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
heartburn relief (source: ndc)
Generic Name
famotidine (source: ndc)
Application Number
ANDA215822 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/1
Packaging
- 1 BOTTLE in 1 PACKAGE (83059-0005-5) / 50 TABLET, FILM COATED in 1 BOTTLE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "458b9ea6-72d7-b5af-e063-6294a90a4430", "openfda": {"nui": ["N0000000151", "N0000175784"], "unii": ["5QZO15J2Z8"], "rxcui": ["199047"], "spl_set_id": ["4e02a443-1e4c-46a5-8323-03d749b8634a"], "pharm_class_epc": ["Histamine-2 Receptor Antagonist [EPC]"], "pharm_class_moa": ["Histamine H2 Receptor Antagonists [MoA]"], "manufacturer_name": ["Shield Pharmaceuticals Corp"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 PACKAGE (83059-0005-5) / 50 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "83059-0005-5", "marketing_start_date": "20240116"}], "brand_name": "Heartburn Relief", "product_id": "83059-0005_458b9ea6-72d7-b5af-e063-6294a90a4430", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H2 Receptor Antagonists [MoA]", "Histamine-2 Receptor Antagonist [EPC]"], "product_ndc": "83059-0005", "generic_name": "Famotidine", "labeler_name": "Shield Pharmaceuticals Corp", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Heartburn Relief", "active_ingredients": [{"name": "FAMOTIDINE", "strength": "10 mg/1"}], "application_number": "ANDA215822", "marketing_category": "ANDA", "marketing_start_date": "20240116", "listing_expiration_date": "20261231"}