NDC 48083-305

CERTI-ANTACID

Calcium Carbonate

CERTI-ANTACID is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by Certified Safety Manufacturing. The primary component is Calcium Carbonate.

Product ID48083-305_1713ce9b-cb23-46de-9344-0251fa284abf
NDC48083-305
Product TypeHuman Otc Drug
Proprietary NameCERTI-ANTACID
Generic NameCalcium Carbonate
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2017-12-29
Marketing CategoryOTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL
Application Numberpart331
Labeler NameCertified Safety Manufacturing
Substance NameCALCIUM CARBONATE
Active Ingredient Strength420 mg/1
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 48083-305-36

250 POUCH in 1 BOX (48083-305-36) > 2 TABLET in 1 POUCH
Marketing Start Date2017-12-29
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 48083-305-36 [48083030536]

CERTI-ANTACID TABLET
Marketing CategoryOTC MONOGRAPH FINAL
Application Numberpart331
Product TypeHUMAN OTC DRUG
Marketing Start Date2017-12-29
Inactivation Date2020-01-31

NDC 48083-305-30 [48083030530]

CERTI-ANTACID TABLET
Marketing CategoryOTC MONOGRAPH FINAL
Application Numberpart331
Product TypeHUMAN OTC DRUG
Marketing Start Date2017-12-29
Inactivation Date2020-01-31

NDC 48083-305-27 [48083030527]

CERTI-ANTACID TABLET
Marketing CategoryOTC MONOGRAPH FINAL
Application Numberpart331
Product TypeHUMAN OTC DRUG
Marketing Start Date2017-12-29
Inactivation Date2020-01-31

NDC 48083-305-33 [48083030533]

CERTI-ANTACID TABLET
Marketing CategoryOTC MONOGRAPH FINAL
Application Numberpart331
Product TypeHUMAN OTC DRUG
Marketing Start Date2017-12-29
Inactivation Date2020-01-31

NDC 48083-305-31 [48083030531]

CERTI-ANTACID TABLET
Marketing CategoryOTC MONOGRAPH FINAL
Application Numberpart331
Product TypeHUMAN OTC DRUG
Marketing Start Date2017-12-29
Inactivation Date2020-01-31

NDC 48083-305-41 [48083030541]

CERTI-ANTACID TABLET
Marketing CategoryOTC MONOGRAPH FINAL
Application Numberpart331
Product TypeHUMAN OTC DRUG
Marketing Start Date2017-12-29
Inactivation Date2020-01-31

NDC 48083-305-39 [48083030539]

CERTI-ANTACID TABLET
Marketing CategoryOTC MONOGRAPH FINAL
Application Numberpart331
Product TypeHUMAN OTC DRUG
Marketing Start Date2017-12-29
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
CALCIUM CARBONATE420 mg/1

OpenFDA Data

SPL SET ID:a3576dc5-5058-4295-a4a1-4550eef12030
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 198529

    • NDC Crossover Matching brand name "CERTI-ANTACID" or generic name "Calcium Carbonate"

    NDCBrand NameGeneric Name
    48083-305CERTI-ANTACIDCERTI-ANTACID
    0113-7489basic care antacidCalcium carbonate
    0113-7595basic care antacidCalcium Carbonate
    0054-3117Calcium CarbonateCalcium Carbonate
    0054-4120Calcium CarbonateCalcium Carbonate
    0054-8120Calcium CarbonateCalcium Carbonate
    0121-0766Calcium CarbonateCalcium Carbonate
    0121-4766Calcium CarbonateCalcium Carbonate
    0113-0009Good Sense Antacidcalcium carbonate
    0113-0179good sense antacidCalcium carbonate
    0113-0468good sense antacidCalcium carbonate
    0113-0478good sense antacidcalcium carbonate
    0113-0485good sense antacidcalcium carbonate
    0113-0489good sense antacidCalcium carbonate
    0113-0595good sense antacidCalcium Carbonate
    0113-0881Good Sense Antacidcalcium carbonate
    0113-0904good sense antacidCalcium carbonate
    0113-0962good sense antacidCalcium carbonate
    0135-0070TUMScalcium carbonate
    0135-0071TUMScalcium carbonate
    0135-0074TUMScalcium carbonate
    0135-0076TUMScalcium carbonate
    0135-0118TUMScalcium carbonate
    0135-0140TUMScalcium carbonate
    0135-0154TUMScalcium carbonate
    0135-0155TUMScalcium carbonate
    0135-0178TUMScalcium carbonate
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