NDC 0113-0571

good sense aller ease

Fexofenadine Hydrochloride

good sense aller ease is a Oral Tablet, Film Coated in the Human Otc Drug category. It is labeled and distributed by L. Perrigo Company. The primary component is Fexofenadine Hydrochloride.

Product ID0113-0571_8e5345ca-5c73-4351-a85d-8976ce33ec7d
NDC0113-0571
Product TypeHuman Otc Drug
Proprietary Namegood sense aller ease
Generic NameFexofenadine Hydrochloride
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2011-04-14
Marketing CategoryANDA / ANDA
Application NumberANDA076447
Labeler NameL. Perrigo Company
Substance NameFEXOFENADINE HYDROCHLORIDE
Active Ingredient Strength180 mg/1
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 0113-0571-22

15 BLISTER PACK in 1 CARTON (0113-0571-22) > 1 TABLET, FILM COATED in 1 BLISTER PACK
Marketing Start Date2011-06-29
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0113-0571-22 [00113057122]

good sense aller ease TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA076447
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2011-06-29

NDC 0113-0571-95 [00113057195]

good sense aller ease TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA076447
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2011-09-20

NDC 0113-0571-76 [00113057176]

good sense aller ease TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA076447
Product TypeHUMAN OTC DRUG
Marketing Start Date2014-04-27
Marketing End Date2018-04-27

NDC 0113-0571-49 [00113057149]

good sense aller ease TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA076447
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-05-23

NDC 0113-0571-39 [00113057139]

good sense aller ease TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA076447
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2011-04-14

Drug Details

Active Ingredients

IngredientStrength
FEXOFENADINE HYDROCHLORIDE180 mg/1

OpenFDA Data

SPL SET ID:4c480f3b-1283-4e9e-bd81-d6e9955d2a1f
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 997420

    • NDC Crossover Matching brand name "good sense aller ease" or generic name "Fexofenadine Hydrochloride"

    NDCBrand NameGeneric Name
    0113-0425Good Sense Aller EaseFexofenadine HCl
    0113-0571good sense aller easefexofenadine hydrochloride
    0113-0847good sense aller easefexofenadine hydrochloride
    10202-107AllergyFexofenadine hydrochloride
    11822-0425allergy relieffexofenadine hydrochloride
    11822-0571allergy relieffexofenadine hydrochloride
    11822-3698Allergy ReliefFexofenadine hydrochloride
    21130-784Allergy ReliefFexofenadine hydrochloride
    0363-0095Fexofenadine hydrochlorideFexofenadine hydrochloride
    0363-0097Fexofenadine hydrochlorideFexofenadine hydrochloride
    0363-0783Fexofenadine hydrochlorideFexofenadine hydrochloride
    0363-9898Fexofenadine HydrochlorideFexofenadine Hydrochloride
    0615-5619Fexofenadine HydrochlorideFexofenadine Hydrochloride
    0615-5620Fexofenadine HydrochlorideFexofenadine Hydrochloride
    0615-7636Fexofenadine HydrochlorideFexofenadine Hydrochloride
    0904-5961Fexofenadine HydrochlorideFexofenadine Hydrochloride
    0904-5962Fexofenadine HydrochlorideFexofenadine Hydrochloride
    0904-5963Fexofenadine HydrochlorideFexofenadine Hydrochloride
    0904-6214fexofenadine hydrochloridefexofenadine hydrochloride
    0904-6711Fexofenadine hydrochlorideFexofenadine hydrochloride
    10202-229Fexofenadine hydrochlorideFexofenadine hydrochloride
    13107-066Fexofenadine hydrochlorideFexofenadine hydrochloride
    13107-067Fexofenadine hydrochlorideFexofenadine hydrochloride
    0179-8325Fexofenadine Hydrochloride 180Fexofenadine Hydrochloride
    11673-571up and up allergy relieffexofenadine hydrochloride
    11673-617up and up allergy relieffexofenadine hydrochloride
    11673-800up and up allergy reliefFexofenadine Hydrochloride
    0363-0571wal fex allergyfexofenadine hydrochloride
    0363-0784Wal-FexFexofenadine hydrochloride
    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.