maximum strength acid reducer

Generic: famotidine

Labeler: time cap laboratories,inc
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name maximum strength acid reducer
Generic Name famotidine
Labeler time cap laboratories,inc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

famotidine 20 mg/1

Manufacturer
TIME CAP LABORATORIES,INC

Identifiers & Regulatory

Product NDC 49483-720
Product ID 49483-720_12f9b308-9375-2df3-e063-6394a90a8d22
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA217543
Listing Expiration 2026-12-31
Marketing Start 2023-06-15

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 49483720
Hyphenated Format 49483-720

Supplemental Identifiers

RxCUI
310273
UPC
0349483720013
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 maximum strength acid reducer (source: ndc)
Generic Name famotidine (source: ndc)
Application Number ANDA217543 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (49483-720-01)
  • 200 TABLET in 1 BOTTLE (49483-720-20)
source: ndc

Packages (2)

49483-720-01 100 TABLET in 1 BOTTLE (49483-720-01) 49483-720-20 200 TABLET in 1 BOTTLE (49483-720-20)

Ingredients (1)

famotidine (20 mg/1)

Linked Drug Pages (1)

Maximum Strength Acid Reducer ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "12f9b308-9375-2df3-e063-6394a90a8d22", "openfda": {"nui": ["N0000000151", "N0000175784"], "upc": ["0349483720013"], "unii": ["5QZO15J2Z8"], "rxcui": ["310273"], "spl_set_id": ["fe25e1e2-7158-6fe0-e053-6394a90a3bb1"], "pharm_class_epc": ["Histamine-2 Receptor Antagonist [EPC]"], "pharm_class_moa": ["Histamine H2 Receptor Antagonists [MoA]"], "manufacturer_name": ["TIME CAP LABORATORIES,INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (49483-720-01)", "package_ndc": "49483-720-01", "marketing_start_date": "20240311"}, {"sample": false, "description": "200 TABLET in 1 BOTTLE (49483-720-20)", "package_ndc": "49483-720-20", "marketing_start_date": "20230615"}], "brand_name": "Maximum Strength Acid Reducer", "product_id": "49483-720_12f9b308-9375-2df3-e063-6394a90a8d22", "dosage_form": "TABLET", "pharm_class": ["Histamine H2 Receptor Antagonists [MoA]", "Histamine-2 Receptor Antagonist [EPC]"], "product_ndc": "49483-720", "generic_name": "Famotidine", "labeler_name": "TIME CAP LABORATORIES,INC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Maximum Strength Acid Reducer", "active_ingredients": [{"name": "FAMOTIDINE", "strength": "20 mg/1"}], "application_number": "ANDA217543", "marketing_category": "ANDA", "marketing_start_date": "20230615", "listing_expiration_date": "20261231"}