NDC 59779-738

Acid Reducer Plus Antacid

Famotidine, Calcium Carbonate And Magnesium Hydroxide

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

Product ID59779-738_62bb0cdc-a218-4608-9b38-d113f293c98c
NDC59779-738
Product TypeHuman Otc Drug
Proprietary NameAcid Reducer Plus Antacid
Generic NameFamotidine, Calcium Carbonate And Magnesium Hydroxide
Dosage FormTablet, Chewable
Route of AdministrationORAL
Marketing Start Date2016-02-11
Marketing CategoryANDA / ANDA
Application NumberANDA077355
Labeler NameCVS Pharmacy
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 59779-738-63

25 TABLET, CHEWABLE in 1 BOTTLE (59779-738-63)
Marketing Start Date2016-02-11
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 59779-738-63 [59779073863]

Acid Reducer Plus Antacid TABLET, CHEWABLE
Marketing CategoryANDA
Application NumberANDA077355
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-02-11

NDC 59779-738-33 [59779073833]

Acid Reducer Plus Antacid TABLET, CHEWABLE
Marketing CategoryANDA
Application NumberANDA077355
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-06-08

NDC 59779-738-71 [59779073871]

Acid Reducer Plus Antacid TABLET, CHEWABLE
Marketing CategoryANDA
Application NumberANDA077355
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-02-11

Drug Details

Active Ingredients

IngredientStrength
FAMOTIDINE10 mg/1

OpenFDA Data

SPL SET ID:509435e4-14fd-4e09-bdc1-ad295b46806b
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 283641
  • NDC Crossover Matching brand name "Acid Reducer Plus Antacid" or generic name "Famotidine, Calcium Carbonate And 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
    0363-0321Acid Controller Completefamotidine, calcium carbonate and magnesium hydroxide
    0363-0511Acid Reducer Completefamotidine, calcium carbonate and magnesium hydroxide
    37012-103Acid Reducer Completefamotidine, calcium carbonate and magnesium hydroxide
    0113-7321basic care dual action completefamotidine, calcium carbonate and magnesium hydroxide
    30142-040Dual Action Completefamotidine, calcium carbonate and magnesium hydroxide
    37808-503Dual Action Completefamotidine, calcium carbonate and magnesium hydroxide
    41163-321equaline completefamotidine, calcium carbonate and magnesium hydroxide
    24385-201good neighbor pharmacy completefamotidine, calcium carbonate and magnesium hydroxide
    0113-0032Good Sense Dual Action Completefamotidine, calcium carbonate and magnesium hydroxide
    0113-6023injoy heartburn relieffamotidine, calcium carbonate and magnesium hydroxide
    37205-680leader acid reducer completefamotidine, calcium carbonate and magnesium hydroxide
    21130-087Signature Care Acid Reducer Completefamotidine, calcium carbonate and magnesium hydroxide
    36800-616topcare dual action completefamotidine, calcium carbonate and magnesium hydroxide
    11673-007up and up famotidine completefamotidine, calcium carbonate and magnesium hydroxide

    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.