NDC 0363-0713

Acid Reducer Complete

Famotidine, Calcium Carbonate, Magnesium Hydroxide

Acid Reducer Complete is a Oral Tablet, Chewable in the Human Otc Drug category. It is labeled and distributed by Walgreen Company. The primary component is Calcium Carbonate; Famotidine; Magnesium Hydroxide.

Product ID0363-0713_02b59032-b352-4001-8be0-a2683fad38e7
NDC0363-0713
Product TypeHuman Otc Drug
Proprietary NameAcid Reducer Complete
Generic NameFamotidine, Calcium Carbonate, Magnesium Hydroxide
Dosage FormTablet, Chewable
Route of AdministrationORAL
Marketing Start Date2016-01-29
Marketing CategoryANDA / ANDA
Application NumberANDA077355
Labeler NameWalgreen Company
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 0363-0713-33

60 TABLET, CHEWABLE in 1 BOTTLE (0363-0713-33)
Marketing Start Date2018-11-19
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0363-0713-63 [00363071363]

Acid Reducer Complete TABLET, CHEWABLE
Marketing CategoryANDA
Application NumberANDA077355
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-01-29

NDC 0363-0713-71 [00363071371]

Acid Reducer Complete TABLET, CHEWABLE
Marketing CategoryANDA
Application NumberANDA077355
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-01-29

NDC 0363-0713-33 [00363071333]

Acid Reducer Complete TABLET, CHEWABLE
Marketing CategoryANDA
Application NumberANDA077355
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-11-19

Drug Details

Active Ingredients

IngredientStrength
FAMOTIDINE10 mg/1

OpenFDA Data

SPL SET ID:6f1dcfda-c12a-4c3b-80a2-c9e15517c88f
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 283641

    • NDC Crossover Matching brand name "Acid Reducer Complete" or generic name "Famotidine, Calcium Carbonate, Magnesium Hydroxide"

    NDCBrand NameGeneric Name
    0363-0511Acid Reducer Completefamotidine, calcium carbonate and magnesium hydroxide
    0363-0713Acid Reducer CompleteFamotidine, Calcium Carbonate, Magnesium Hydroxide
    37012-009Acid Reducer CompleteFamotidine, Calcium Carbonate, Magnesium Hydroxide
    37012-103Acid Reducer Completefamotidine, calcium carbonate and magnesium hydroxide
    55319-399acid reducer completeacid reducer complete
    11822-0223acid reducer plus antacidFamotidine, 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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