acid reducer complete
Generic: famotidine, calcium carbonate, magnesium hydroxide
Labeler: safewayDrug Facts
Product Profile
Brand Name
acid reducer complete
Generic Name
famotidine, calcium carbonate, magnesium hydroxide
Labeler
safeway
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
21130-786
Product ID
21130-786_323b0cda-6d60-4877-97e6-4f60552642c0
Product Type
HUMAN OTC DRUG
Marketing Category
ANDA
Application Number
ANDA077355
Listing Expiration
2026-12-31
Marketing Start
2025-09-22
Pharmacologic Class
Established (EPC)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
21130786
Hyphenated Format
21130-786
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
acid reducer complete (source: ndc)
Generic Name
famotidine, calcium carbonate, 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 (21130-786-63)
- 50 TABLET, CHEWABLE in 1 BOTTLE (21130-786-71)
Packages (2)
Ingredients (3)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "323b0cda-6d60-4877-97e6-4f60552642c0", "openfda": {"nui": ["N0000000151", "N0000175784"], "unii": ["H0G9379FGK", "5QZO15J2Z8", "NBZ3QY004S"], "rxcui": ["283641"], "spl_set_id": ["4f0a178c-d0ed-4bbc-a8ce-fda3789d25f0"], "pharm_class_epc": ["Histamine-2 Receptor Antagonist [EPC]"], "pharm_class_moa": ["Histamine H2 Receptor Antagonists [MoA]"], "manufacturer_name": ["Safeway"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 TABLET, CHEWABLE in 1 BOTTLE (21130-786-63)", "package_ndc": "21130-786-63", "marketing_start_date": "20250929"}, {"sample": false, "description": "50 TABLET, CHEWABLE in 1 BOTTLE (21130-786-71)", "package_ndc": "21130-786-71", "marketing_start_date": "20250922"}], "brand_name": "acid reducer complete", "product_id": "21130-786_323b0cda-6d60-4877-97e6-4f60552642c0", "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": "21130-786", "generic_name": "Famotidine, Calcium Carbonate, Magnesium Hydroxide", "labeler_name": "Safeway", "product_type": "HUMAN OTC DRUG", "brand_name_base": "acid reducer complete", "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": "20250922", "listing_expiration_date": "20261231"}