NDC 11822-0223

acid reducer plus antacid

Famotidine, Calcium Carbonate, Magnesium Hydroxide

acid reducer plus antacid is a Oral Tablet, Chewable in the Human Otc Drug category. It is labeled and distributed by Rite Aid Corporation. The primary component is Calcium Carbonate; Famotidine; Magnesium Hydroxide.

Product ID11822-0223_bb2a0e3a-ac9d-42a3-90e1-8b6195023b8b
NDC11822-0223
Product TypeHuman Otc Drug
Proprietary Nameacid reducer plus antacid
Generic NameFamotidine, Calcium Carbonate, Magnesium Hydroxide
Dosage FormTablet, Chewable
Route of AdministrationORAL
Marketing Start Date2010-06-03
Marketing CategoryANDA / ANDA
Application NumberANDA077355
Labeler NameRite Aid Corporation
Substance NameCALCIUM CARBONATE; FAMOTIDINE; MAGNESIUM HYDROXIDE
Active Ingredient Strength800 mg/1; mg/1; mg/1
Pharm ClassesCalculi 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]
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 11822-0223-0

50 TABLET, CHEWABLE in 1 BOTTLE (11822-0223-0)
Marketing Start Date2010-06-03
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 11822-0223-1 [11822022301]

acid reducer plus antacid TABLET, CHEWABLE
Marketing CategoryANDA
Application NumberANDA077355
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-06-03
Marketing End Date2016-10-05

NDC 11822-0223-0 [11822022300]

acid reducer plus antacid TABLET, CHEWABLE
Marketing CategoryANDA
Application NumberANDA077355
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-06-03

Drug Details

Active Ingredients

IngredientStrength
FAMOTIDINE10 mg/1

OpenFDA Data

SPL SET ID:c64c7100-4b2d-4994-8f30-be1a88a97358
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 283641

    • NDC Crossover Matching brand name "acid reducer plus antacid" or generic name "Famotidine, Calcium Carbonate, Magnesium Hydroxide"

    NDCBrand NameGeneric Name
    11822-0223acid reducer plus antacidFamotidine, Calcium Carbonate, Magnesium Hydroxide
    11822-0500Acid Reducer Plus Antacidfamotidine, calcium carbonate and magnesium hydroxide
    69842-802acid reducer plus antacidacid reducer plus antacid
    59779-738Acid Reducer Plus AntacidAcid Reducer Plus Antacid
    59779-862Acid Reducer Plus AntacidAcid Reducer Plus Antacid
    0363-0713Acid Reducer CompleteFamotidine, Calcium Carbonate, Magnesium Hydroxide
    37012-009Acid Reducer CompleteFamotidine, Calcium Carbonate, Magnesium Hydroxide
    41520-617CareOne Acid Reducer CompleteFamotidine, Calcium Carbonate, Magnesium Hydroxide
    30142-213Dual Action CompleteFamotidine, Calcium Carbonate, Magnesium Hydroxide
    37808-121Dual Action CompleteFamotidine, Calcium Carbonate, Magnesium Hydroxide
    41250-690Dual Action CompleteFamotidine, Calcium Carbonate, Magnesium Hydroxide
    0597-0315DUO FusionFamotidine, Calcium carbonate, Magnesium hydroxide
    0597-0320DUO FusionFamotidine, Calcium carbonate, Magnesium hydroxide
    41163-546equaline completeFamotidine, Calcium Carbonate, Magnesium Hydroxide
    37205-681leader acid reducer completeFamotidine, Calcium Carbonate, Magnesium Hydroxide
    21130-546signature care acid reducer completeFamotidine, Calcium Carbonate, Magnesium Hydroxide
    36800-082topcare dual action completeFamotidine, Calcium Carbonate, Magnesium Hydroxide
    11673-010up and up famotidine completeFamotidine, Calcium Carbonate, Magnesium Hydroxide
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