NDC 16837-855

PEPCID AC Maximum Strength

Famotidine

PEPCID AC Maximum Strength is a Oral Tablet, Film Coated in the Human Otc Drug category. It is labeled and distributed by Johnson & Johnson Consumer Inc., Mcneil Consumer Healthcare Division. The primary component is Famotidine.

Product ID16837-855_03eabe8f-7603-4cc8-93cf-a3b5b795ba51
NDC16837-855
Product TypeHuman Otc Drug
Proprietary NamePEPCID AC Maximum Strength
Generic NameFamotidine
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2003-09-01
Marketing CategoryNDA / NDA
Application NumberNDA020325
Labeler NameJohnson & Johnson Consumer Inc., McNeil Consumer Healthcare Division
Substance NameFAMOTIDINE
Active Ingredient Strength20 mg/1
NDC Exclude FlagN
Listing Certified Through2022-12-31

Packaging

NDC 16837-855-05

1 BLISTER PACK in 1 CARTON (16837-855-05) > 5 TABLET, FILM COATED in 1 BLISTER PACK
Marketing Start Date2003-09-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 16837-855-12 [16837085512]

PEPCID AC Maximum Strength TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA020325
Product TypeHUMAN OTC DRUG
Marketing Start Date2003-09-01

NDC 16837-855-26 [16837085526]

PEPCID AC Maximum Strength TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA020325
Product TypeHUMAN OTC DRUG
Marketing Start Date2003-09-01
Marketing End Date2010-12-07

NDC 16837-855-70 [16837085570]

PEPCID AC Maximum Strength TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA020325
Product TypeHUMAN OTC DRUG
Marketing Start Date2003-09-01

NDC 16837-855-49 [16837085549]

PEPCID AC Maximum Strength TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA020325
Product TypeHUMAN OTC DRUG
Marketing Start Date2003-09-01

NDC 16837-855-08 [16837085508]

PEPCID AC Maximum Strength TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA020325
Product TypeHUMAN OTC DRUG
Marketing Start Date2003-09-01
Marketing End Date2015-04-27

NDC 16837-855-16 [16837085516]

PEPCID AC Maximum Strength TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA020325
Product TypeHUMAN OTC DRUG
Marketing Start Date2003-09-01

NDC 16837-855-13 [16837085513]

PEPCID AC Maximum Strength TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA020325
Product TypeHUMAN OTC DRUG
Marketing Start Date2003-09-01

NDC 16837-855-25 [16837085525]

PEPCID AC Maximum Strength TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA020325
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2003-09-01
Marketing End Date2014-03-31

NDC 16837-855-17 [16837085517]

PEPCID AC Maximum Strength TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA020325
Product TypeHUMAN OTC DRUG
Marketing Start Date2003-09-01

NDC 16837-855-67 [16837085567]

PEPCID AC Maximum Strength TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA020325
Product TypeHUMAN OTC DRUG
Marketing Start Date2003-09-01

NDC 16837-855-51 [16837085551]

PEPCID AC Maximum Strength TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA020325
Product TypeHUMAN OTC DRUG
Marketing Start Date2003-09-01

NDC 16837-855-09 [16837085509]

PEPCID AC Maximum Strength TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA020325
Product TypeHUMAN OTC DRUG
Marketing Start Date2003-09-01

NDC 16837-855-85 [16837085585]

PEPCID AC Maximum Strength TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA020325
Product TypeHUMAN OTC DRUG
Marketing Start Date2003-09-01

NDC 16837-855-18 [16837085518]

PEPCID AC Maximum Strength TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA020325
Product TypeHUMAN OTC DRUG
Marketing Start Date2003-09-01

NDC 16837-855-11 [16837085511]

PEPCID AC Maximum Strength TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA020325
Product TypeHUMAN OTC DRUG
Marketing Start Date2003-09-01
Marketing End Date2010-12-07

NDC 16837-855-80 [16837085580]

PEPCID AC Maximum Strength TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA020325
Product TypeHUMAN OTC DRUG
Marketing Start Date2003-09-01

NDC 16837-855-52 [16837085552]

PEPCID AC Maximum Strength TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA020325
Product TypeHUMAN OTC DRUG
Marketing Start Date2003-09-01

NDC 16837-855-65 [16837085565]

PEPCID AC Maximum Strength TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA020325
Product TypeHUMAN OTC DRUG
Marketing Start Date2003-09-01

NDC 16837-855-20 [16837085520]

PEPCID AC Maximum Strength TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA020325
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2014-08-22

NDC 16837-855-15 [16837085515]

PEPCID AC Maximum Strength TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA020325
Product TypeHUMAN OTC DRUG
Marketing Start Date2003-09-01

NDC 16837-855-40 [16837085540]

PEPCID AC Maximum Strength TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA020325
Product TypeHUMAN OTC DRUG
Marketing Start Date2003-09-01

NDC 16837-855-19 [16837085519]

PEPCID AC Maximum Strength TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA020325
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-04-27

NDC 16837-855-28 [16837085528]

PEPCID AC Maximum Strength TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA020325
Product TypeHUMAN OTC DRUG
Marketing Start Date2003-09-01
Marketing End Date2015-12-15

NDC 16837-855-50 [16837085550]

PEPCID AC Maximum Strength TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA020325
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2003-09-01

NDC 16837-855-75 [16837085575]

PEPCID AC Maximum Strength TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA020325
Product TypeHUMAN OTC DRUG
Marketing Start Date2003-09-01

NDC 16837-855-05 [16837085505]

PEPCID AC Maximum Strength TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA020325
Product TypeHUMAN OTC DRUG
Marketing Start Date2003-09-01

NDC 16837-855-42 [16837085542]

PEPCID AC Maximum Strength TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA020325
Product TypeHUMAN OTC DRUG
Marketing Start Date2003-09-01
Marketing End Date2010-12-07

NDC 16837-855-14 [16837085514]

PEPCID AC Maximum Strength TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA020325
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2003-09-01

NDC 16837-855-64 [16837085564]

PEPCID AC Maximum Strength TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA020325
Product TypeHUMAN OTC DRUG
Marketing Start Date2003-09-01
Marketing End Date2015-12-15

Drug Details

Active Ingredients

IngredientStrength
FAMOTIDINE20 mg/1

OpenFDA Data

SPL SET ID:2854047f-c5c4-43c3-8ef2-5c0a84a307f2
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 310273
  • 104094
  • NDC Crossover Matching brand name "PEPCID AC Maximum Strength" or generic name "Famotidine"

    NDCBrand NameGeneric Name
    16837-855PEPCID AC Maximum StrengthPEPCID AC Maximum Strength
    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

    Trademark Results [PEPCID AC]

    Mark Image

    Registration | Serial
    Company
    Trademark
    Application Date
    PEPCID AC
    PEPCID AC
    74565086 1984651 Live/Registered
    JOHNSON & JOHNSON
    1994-08-24
    PEPCID AC
    PEPCID AC
    74242973 1812672 Dead/Cancelled
    MERCK & CO., Inc.
    1992-02-03

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