heartburn relief original strength

Generic: famotidine

Labeler: proficient rx lp
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name heartburn relief original strength
Generic Name famotidine
Labeler proficient rx lp
Dosage Form TABLET
Routes
ORAL
Active Ingredients

famotidine 10 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 63187-999
Product ID 63187-999_6df77a1c-accd-4559-9a9a-00a030f6ba64
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA075400
Listing Expiration 2026-12-31
Marketing Start 2009-09-09

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 63187999
Hyphenated Format 63187-999

Supplemental Identifiers

RxCUI
199047
UNII
5QZO15J2Z8
NUI
N0000000151 N0000175784

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 original strength (source: ndc)
Generic Name famotidine (source: ndc)
Application Number ANDA075400 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 10 TABLET in 1 BOTTLE (63187-999-10)
  • 30 TABLET in 1 BOTTLE (63187-999-30)
  • 60 TABLET in 1 BOTTLE (63187-999-60)
  • 90 TABLET in 1 BOTTLE (63187-999-90)
source: ndc

Packages (4)

Ingredients (1)

famotidine (10 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "6df77a1c-accd-4559-9a9a-00a030f6ba64", "openfda": {"nui": ["N0000000151", "N0000175784"], "unii": ["5QZO15J2Z8"], "rxcui": ["199047"], "spl_set_id": ["5567aaaf-b4f2-4604-b841-c9447e77256c"], "pharm_class_epc": ["Histamine-2 Receptor Antagonist [EPC]"], "pharm_class_moa": ["Histamine H2 Receptor Antagonists [MoA]"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET in 1 BOTTLE (63187-999-10)", "package_ndc": "63187-999-10", "marketing_start_date": "20180402"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (63187-999-30)", "package_ndc": "63187-999-30", "marketing_start_date": "20180402"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (63187-999-60)", "package_ndc": "63187-999-60", "marketing_start_date": "20180402"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (63187-999-90)", "package_ndc": "63187-999-90", "marketing_start_date": "20180402"}], "brand_name": "heartburn relief original strength", "product_id": "63187-999_6df77a1c-accd-4559-9a9a-00a030f6ba64", "dosage_form": "TABLET", "pharm_class": ["Histamine H2 Receptor Antagonists [MoA]", "Histamine-2 Receptor Antagonist [EPC]"], "product_ndc": "63187-999", "generic_name": "Famotidine", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN OTC DRUG", "brand_name_base": "heartburn relief", "brand_name_suffix": "original strength", "active_ingredients": [{"name": "FAMOTIDINE", "strength": "10 mg/1"}], "application_number": "ANDA075400", "marketing_category": "ANDA", "marketing_start_date": "20090909", "listing_expiration_date": "20261231"}