NDC 16837-872

Pepcid AC Original Strength

Famotidine

Pepcid AC Original 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 ID16837-872_1f1c9532-332b-4c72-baa1-04f3d0d8150e
NDC16837-872
Product TypeHuman Otc Drug
Proprietary NamePepcid AC Original Strength
Generic NameFamotidine
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date1995-10-01
Marketing CategoryNDA / NDA
Application NumberNDA020325
Labeler NameJohnson & Johnson Consumer Inc., McNeil Consumer Healthcare Division
Substance NameFAMOTIDINE
Active Ingredient Strength10 mg/1
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 16837-872-10

1 BLISTER PACK in 1 CARTON (16837-872-10) > 10 TABLET, FILM COATED in 1 BLISTER PACK
Marketing Start Date2011-01-21
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 16837-872-60 [16837087260]

Pepcid AC Original Strength TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA020325
Product TypeHUMAN OTC DRUG
Marketing Start Date1995-10-01

NDC 16837-872-61 [16837087261]

Pepcid AC Original Strength TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA020325
Product TypeHUMAN OTC DRUG
Marketing Start Date1995-10-01
Marketing End Date2011-03-10

NDC 16837-872-64 [16837087264]

Pepcid AC Original Strength TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA020325
Product TypeHUMAN OTC DRUG
Marketing Start Date1995-10-01
Marketing End Date2011-03-10

NDC 16837-872-18 [16837087218]

Pepcid AC Original Strength TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA020325
Product TypeHUMAN OTC DRUG
Marketing Start Date1995-10-01
Marketing End Date2011-03-10

NDC 16837-872-12 [16837087212]

Pepcid AC Original Strength TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA020325
Product TypeHUMAN OTC DRUG
Marketing Start Date1995-10-01
Marketing End Date2011-03-10

NDC 16837-872-90 [16837087290]

Pepcid AC Original Strength TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA020325
Product TypeHUMAN OTC DRUG
Marketing Start Date1995-10-01

NDC 16837-872-10 [16837087210]

Pepcid AC Original Strength TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA020325
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-01-21

NDC 16837-872-31 [16837087231]

Pepcid AC Original Strength TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA020325
Product TypeHUMAN OTC DRUG
Marketing Start Date1995-10-01

NDC 16837-872-91 [16837087291]

Pepcid AC Original Strength TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA020325
Product TypeHUMAN OTC DRUG
Marketing Start Date1995-10-01
Marketing End Date2011-03-10

NDC 16837-872-21 [16837087221]

Pepcid AC Original Strength TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA020325
Product TypeHUMAN OTC DRUG
Marketing Start Date1995-10-01
Marketing End Date2015-12-16

NDC 16837-872-20 [16837087220]

Pepcid AC Original Strength TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA020325
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-01-21

NDC 16837-872-06 [16837087206]

Pepcid AC Original Strength TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA020325
Product TypeHUMAN OTC DRUG
Marketing Start Date1995-10-01
Marketing End Date2014-11-18

NDC 16837-872-30 [16837087230]

Pepcid AC Original Strength TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA020325
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date1995-10-01

NDC 16837-872-22 [16837087222]

Pepcid AC Original Strength TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA020325
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-01-21

NDC 16837-872-50 [16837087250]

Pepcid AC Original Strength TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA020325
Product TypeHUMAN OTC DRUG
Marketing Start Date1995-10-01
Marketing End Date2011-03-10

Drug Details

Active Ingredients

IngredientStrength
FAMOTIDINE10 mg/1

OpenFDA Data

SPL SET ID:54f4086f-e443-4e7e-8c7e-94e152e1c256
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 199047
  • 212072
  • NDC Crossover Matching brand name "Pepcid AC Original Strength" or generic name "Famotidine"

    NDCBrand NameGeneric Name
    16837-872Pepcid AC Original StrengthPepcid AC Original 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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