heartburn prevention

Generic: famotidine

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

Drug Facts

Product Profile

Brand Name heartburn prevention
Generic Name famotidine
Labeler kroger company
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

famotidine 20 mg/1

Manufacturer
Kroger Company

Identifiers & Regulatory

Product NDC 30142-194
Product ID 30142-194_c1cf5e39-9332-4823-9c3f-f6976bda5b1c
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA077351
Listing Expiration 2026-12-31
Marketing Start 2015-02-05

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 30142194
Hyphenated Format 30142-194

Supplemental Identifiers

RxCUI
310273
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 heartburn prevention (source: ndc)
Generic Name famotidine (source: ndc)
Application Number ANDA077351 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (30142-194-01) / 85 TABLET, FILM COATED in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (30142-194-71) / 50 TABLET, FILM COATED in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (30142-194-98) / 75 TABLET, FILM COATED in 1 BOTTLE
source: ndc

Packages (3)

Ingredients (1)

famotidine (20 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "c1cf5e39-9332-4823-9c3f-f6976bda5b1c", "openfda": {"nui": ["N0000000151", "N0000175784"], "unii": ["5QZO15J2Z8"], "rxcui": ["310273"], "spl_set_id": ["c97851ef-7b49-4f6c-b165-147555db101a"], "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": "1 BOTTLE in 1 CARTON (30142-194-01)  / 85 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "30142-194-01", "marketing_start_date": "20240521"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (30142-194-71)  / 50 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "30142-194-71", "marketing_start_date": "20150205"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (30142-194-98)  / 75 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "30142-194-98", "marketing_start_date": "20250414"}], "brand_name": "heartburn prevention", "product_id": "30142-194_c1cf5e39-9332-4823-9c3f-f6976bda5b1c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H2 Receptor Antagonists [MoA]", "Histamine-2 Receptor Antagonist [EPC]"], "product_ndc": "30142-194", "generic_name": "Famotidine", "labeler_name": "Kroger Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "heartburn prevention", "active_ingredients": [{"name": "FAMOTIDINE", "strength": "20 mg/1"}], "application_number": "ANDA077351", "marketing_category": "ANDA", "marketing_start_date": "20150205", "listing_expiration_date": "20261231"}