NDC 0363-0049

Fexofenadine HCl and Pseudoephedrine HCl

Fexofenadine Hcl And Pseudoephedrine Hcl

Fexofenadine HCl and Pseudoephedrine HCl is a Oral Tablet, Extended Release in the Human Otc Drug category. It is labeled and distributed by Walgreens Company. The primary component is Fexofenadine Hydrochloride; Pseudoephedrine Hydrochloride.

Product ID0363-0049_52643946-ec2b-c2bf-7180-d666266ca0f4
NDC0363-0049
Product TypeHuman Otc Drug
Proprietary NameFexofenadine HCl and Pseudoephedrine HCl
Generic NameFexofenadine Hcl And Pseudoephedrine Hcl
Dosage FormTablet, Extended Release
Route of AdministrationORAL
Marketing Start Date2022-07-13
Marketing CategoryANDA /
Application NumberANDA079043
Labeler NameWalgreens company
Substance NameFEXOFENADINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE
Active Ingredient Strength180 mg/1; mg/1
Pharm ClassesAdrenergic alpha-Agonists [MoA], Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC], alpha-Adrenergic Agonist [EPC]
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 0363-0049-10

2 BLISTER PACK in 1 CARTON (0363-0049-10) > 5 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
Marketing Start Date2022-07-13
NDC Exclude FlagN
Sample Package?N

Drug Details

NDC Crossover Matching brand name "Fexofenadine HCl and Pseudoephedrine HCl" or generic name "Fexofenadine Hcl And Pseudoephedrine Hcl"

NDCBrand NameGeneric Name
0363-0049Fexofenadine HCl and Pseudoephedrine HClFexofenadine HCl and Pseudoephedrine HCl
11822-0007Fexofenadine HCl and Pseudoephedrine HClFexofenadine HCl and Pseudoephedrine HCl
43598-892Fexofenadine HCl and Pseudoephedrine HClFexofenadine HCl and Pseudoephedrine HCl
51316-018Fexofenadine HCl and Pseudoephedrine HClFexofenadine HCl and Pseudoephedrine HCl
55111-572Fexofenadine HCl and Pseudoephedrine HClFexofenadine HCl and Pseudoephedrine HCl
70000-0607Fexofenadine HCl and Pseudoephedrine HClFexofenadine HCl and Pseudoephedrine HCl

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