Label: FEXOFENADINE HYDROCHLORIDE tablet, film coated
- NDC Code(s): 71205-739-30, 71205-739-60, 71205-739-90
- Packager: Proficient Rx LP
- This is a repackaged label.
- Source NDC Code(s): 45802-847
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated December 1, 2022
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- Official Label (Printer Friendly)
- Active ingredient (in each tablet)
- Purpose
- Uses
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Warnings
Ask a doctor before use if you have
kidney disease. Your doctor should determine if you need a different dose.
When using this product
- •
- do not take more than directed
- •
- do not take at the same time as aluminum or magnesium antacids
- •
- do not take with fruit juices (see Directions)
- Directions
- Other information
- Inactive ingredients
- Questions or comments?
- Package/Label Principal Display Panel
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INGREDIENTS AND APPEARANCE
FEXOFENADINE HYDROCHLORIDE
fexofenadine hydrochloride tablet, film coatedProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71205-739(NDC:45802-847) Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength FEXOFENADINE HYDROCHLORIDE (UNII: 2S068B75ZU) (FEXOFENADINE - UNII:E6582LOH6V) FEXOFENADINE HYDROCHLORIDE 180 mg Inactive Ingredients Ingredient Name Strength CROSCARMELLOSE SODIUM (UNII: M28OL1HH48) FD&C BLUE NO. 2 (UNII: L06K8R7DQK) FD&C RED NO. 40 (UNII: WZB9127XOA) FD&C YELLOW NO. 6 (UNII: H77VEI93A8) LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X) MAGNESIUM STEARATE (UNII: 70097M6I30) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A) POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990) TALC (UNII: 7SEV7J4R1U) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) Product Characteristics Color PINK Score no score Shape OVAL Size 18mm Flavor Imprint Code L847 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71205-739-30 30 in 1 BOTTLE; Type 0: Not a Combination Product 12/28/2022 2 NDC:71205-739-60 60 in 1 BOTTLE; Type 0: Not a Combination Product 12/28/2022 3 NDC:71205-739-90 90 in 1 BOTTLE; Type 0: Not a Combination Product 12/28/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA212971 01/07/2022 Labeler - Proficient Rx LP (079196022) Establishment Name Address ID/FEI Business Operations Proficient Rx LP 079196022 REPACK(71205-739) , RELABEL(71205-739)