NDC 70925-194

Humana Pharmacy Acid Reducer

Famotidine

Humana Pharmacy Acid Reducer is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by Humana Pharmacy, Inc.. The primary component is Famotidine.

Product ID70925-194_6e9cb258-cf43-42d8-b5c4-4282c73f9b9c
NDC70925-194
Product TypeHuman Otc Drug
Proprietary NameHumana Pharmacy Acid Reducer
Generic NameFamotidine
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2016-12-21
Marketing CategoryANDA / ANDA
Application NumberANDA077351
Labeler NameHumana Pharmacy, Inc.
Substance NameFAMOTIDINE
Active Ingredient Strength20 mg/1
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 70925-194-02

25 BLISTER PACK in 1 CARTON (70925-194-02) > 1 TABLET in 1 BLISTER PACK
Marketing Start Date2016-12-21
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 70925-194-02 [70925019402]

Humana Pharmacy Acid Reducer TABLET
Marketing CategoryANDA
Application NumberANDA077351
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-12-21

Drug Details

Active Ingredients

IngredientStrength
FAMOTIDINE20 mg/1

OpenFDA Data

SPL SET ID:6e9cb258-cf43-42d8-b5c4-4282c73f9b9c
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 310273
  • NDC Crossover Matching brand name "Humana Pharmacy Acid Reducer" or generic name "Famotidine"

    NDCBrand NameGeneric Name
    70925-194Humana Pharmacy Acid ReducerHumana Pharmacy Acid Reducer
    0363-0141Acid ControllerFamotidine
    0363-0701Acid ControllerFamotidine
    0363-1203acid controllerfamotidine
    0113-7141basic care acid reducerFamotidine
    0113-7194Basic Care famotidineFamotidine
    0093-2748FamotidineFamotidine
    0172-5728FamotidineFamotidine
    0172-5729FamotidineFamotidine
    0338-5197FamotidineFamotidine
    0363-0036FamotidineFamotidine
    0363-1899FamotidineFamotidine
    0113-0141good sense acid reducerFamotidine
    0113-0194Good Sense Acid ReducerFamotidine
    0187-4420Pepcidfamotidine
    0187-4440Pepcidfamotidine

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