original strength heartburn prevention

Generic: famotidine

Labeler: kroger company
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name original strength heartburn prevention
Generic Name famotidine
Labeler kroger company
Dosage Form TABLET
Routes
ORAL
Active Ingredients

famotidine 10 mg/1

Manufacturer
KROGER COMPANY

Identifiers & Regulatory

Product NDC 41226-719
Product ID 41226-719_1cb86ee4-41c1-1196-e063-6394a90a9199
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA217543
Listing Expiration 2026-12-31
Marketing Start 2023-05-05

Pharmacologic Class

Established (EPC)
histamine-2 receptor antagonist [epc]
Mechanism of Action
histamine h2 receptor antagonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 41226719
Hyphenated Format 41226-719

Supplemental Identifiers

RxCUI
199047
UPC
0041260018459
UNII
5QZO15J2Z8
NUI
N0000000151 N0000175784

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 original strength heartburn prevention (source: ndc)
Generic Name famotidine (source: ndc)
Application Number ANDA217543 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 3 BLISTER PACK in 1 CARTON (41226-719-06) / 10 TABLET in 1 BLISTER PACK
  • 1 BOTTLE in 1 CARTON (41226-719-09) / 90 TABLET in 1 BOTTLE
source: ndc

Packages (2)

41226-719-06 3 BLISTER PACK in 1 CARTON (41226-719-06) / 10 TABLET in 1 BLISTER PACK 41226-719-09 1 BOTTLE in 1 CARTON (41226-719-09) / 90 TABLET in 1 BOTTLE

Ingredients (1)

famotidine (10 mg/1)

Linked Drug Pages (1)

Original strength heartburn prevention ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "1cb86ee4-41c1-1196-e063-6394a90a9199", "openfda": {"nui": ["N0000000151", "N0000175784"], "upc": ["0041260018459"], "unii": ["5QZO15J2Z8"], "rxcui": ["199047"], "spl_set_id": ["ea1c2838-acbd-18e0-e053-2a95a90a3522"], "pharm_class_epc": ["Histamine-2 Receptor Antagonist [EPC]"], "pharm_class_moa": ["Histamine H2 Receptor Antagonists [MoA]"], "manufacturer_name": ["KROGER COMPANY"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3 BLISTER PACK in 1 CARTON (41226-719-06)  / 10 TABLET in 1 BLISTER PACK", "package_ndc": "41226-719-06", "marketing_start_date": "20230505"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (41226-719-09)  / 90 TABLET in 1 BOTTLE", "package_ndc": "41226-719-09", "marketing_start_date": "20240415"}], "brand_name": "Original strength heartburn prevention", "product_id": "41226-719_1cb86ee4-41c1-1196-e063-6394a90a9199", "dosage_form": "TABLET", "pharm_class": ["Histamine H2 Receptor Antagonists [MoA]", "Histamine-2 Receptor Antagonist [EPC]"], "product_ndc": "41226-719", "generic_name": "Famotidine", "labeler_name": "KROGER COMPANY", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Original strength heartburn prevention", "active_ingredients": [{"name": "FAMOTIDINE", "strength": "10 mg/1"}], "application_number": "ANDA217543", "marketing_category": "ANDA", "marketing_start_date": "20230505", "listing_expiration_date": "20261231"}