equaline complete dual action
Generic: famotidine, calcium carbonate and magnesium hydroxide
Labeler: united natural foods, inc. dba unfiDrug Facts
Product Profile
Brand Name
equaline complete dual action
Generic Name
famotidine, calcium carbonate and magnesium hydroxide
Labeler
united natural foods, inc. dba unfi
Dosage Form
TABLET, CHEWABLE
Routes
Active Ingredients
calcium carbonate 800 mg/1, famotidine 10 mg/1, magnesium hydroxide 165 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
41163-321
Product ID
41163-321_98d04d1a-a80a-419d-b767-3f18655e9867
Product Type
HUMAN OTC DRUG
Marketing Category
ANDA
Application Number
ANDA077355
Listing Expiration
2027-12-31
Marketing Start
2008-09-02
Pharmacologic Class
Established (EPC)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
41163321
Hyphenated Format
41163-321
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
equaline complete dual action (source: ndc)
Generic Name
famotidine, calcium carbonate and magnesium hydroxide (source: ndc)
Application Number
ANDA077355 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 800 mg/1
- 10 mg/1
- 165 mg/1
Packaging
- 25 TABLET, CHEWABLE in 1 BOTTLE (41163-321-63)
Packages (1)
Ingredients (3)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "98d04d1a-a80a-419d-b767-3f18655e9867", "openfda": {"nui": ["N0000000151", "N0000175784"], "unii": ["H0G9379FGK", "5QZO15J2Z8", "NBZ3QY004S"], "rxcui": ["283641"], "spl_set_id": ["c32cb5be-e1f8-4510-8685-5e03a7d4224c"], "pharm_class_epc": ["Histamine-2 Receptor Antagonist [EPC]"], "pharm_class_moa": ["Histamine H2 Receptor Antagonists [MoA]"], "manufacturer_name": ["United Natural Foods, Inc. dba UNFI"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 TABLET, CHEWABLE in 1 BOTTLE (41163-321-63)", "package_ndc": "41163-321-63", "marketing_start_date": "20080902"}], "brand_name": "equaline complete dual action", "product_id": "41163-321_98d04d1a-a80a-419d-b767-3f18655e9867", "dosage_form": "TABLET, CHEWABLE", "pharm_class": ["Calculi Dissolution Agent [EPC]", "Histamine H2 Receptor Antagonists [MoA]", "Histamine-2 Receptor Antagonist [EPC]", "Increased Large Intestinal Motility [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Inhibition Small Intestine Fluid/Electrolyte Absorption [PE]", "Magnesium Ion Exchange Activity [MoA]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]", "Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]"], "product_ndc": "41163-321", "generic_name": "famotidine, calcium carbonate and magnesium hydroxide", "labeler_name": "United Natural Foods, Inc. dba UNFI", "product_type": "HUMAN OTC DRUG", "brand_name_base": "equaline complete", "brand_name_suffix": "dual action", "active_ingredients": [{"name": "CALCIUM CARBONATE", "strength": "800 mg/1"}, {"name": "FAMOTIDINE", "strength": "10 mg/1"}, {"name": "MAGNESIUM HYDROXIDE", "strength": "165 mg/1"}], "application_number": "ANDA077355", "marketing_category": "ANDA", "marketing_start_date": "20080902", "listing_expiration_date": "20271231"}