Label: FEXOFENADINE HCL tablet
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NDC Code(s):
0363-9760-03,
0363-9760-07,
0363-9760-14,
0363-9760-18, view more0363-9760-34
- Packager: Walgreens
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: Abbreviated New Drug Application
Drug Label Information
Updated December 16, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient (in each tablet)
- Purpose
- Uses
- Warnings
- Ask a doctor before use if you have
- When using this product
- Stop use and ask a doctor if
- If pregnant or breast-feeding,
- Keep out of reach of children.
- Directions
- Other information
- Inactive ingredients
- Questions or comments?
- PDP
-
INGREDIENTS AND APPEARANCE
FEXOFENADINE HCL
fexofenadine hcl tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0363-9760 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 STARCH, CORN (UNII: O8232NY3SJ) FERRIC OXIDE RED (UNII: 1K09F3G675) FERROSOFERRIC OXIDE (UNII: XM0M87F357) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) MAGNESIUM STEARATE (UNII: 70097M6I30) LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X) CROSCARMELLOSE SODIUM (UNII: M28OL1HH48) POLYETHYLENE GLYCOL 6000 (UNII: 30IQX730WE) FERRIC OXIDE YELLOW (UNII: EX438O2MRT) HYPROMELLOSE 2910 (15 MPA.S) (UNII: 36SFW2JZ0W) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) Product Characteristics Color orange ((PEACH)) Score no score Shape OVAL ((Capsule-shaped)) Size 17mm Flavor Imprint Code G6 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0363-9760-03 30 in 1 BOTTLE; Type 0: Not a Combination Product 02/28/2024 2 NDC:0363-9760-18 180 in 1 BOTTLE; Type 0: Not a Combination Product 02/28/2024 3 NDC:0363-9760-07 15 in 1 BLISTER PACK; Type 0: Not a Combination Product 02/28/2024 4 NDC:0363-9760-14 5 in 1 BLISTER PACK; Type 0: Not a Combination Product 02/28/2024 5 NDC:0363-9760-34 70 in 1 BOTTLE; Type 0: Not a Combination Product 02/28/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA211075 02/28/2024 Labeler - Walgreens (008965063)