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NDC 70010-0183-03 Fexofenadine HCL 180 mg/1 Details

Fexofenadine HCL 180 mg/1

Fexofenadine HCL is a ORAL TABLET in the HUMAN OTC DRUG category. It is labeled and distributed by GRANULES PHARMACEUTICALS INC.. The primary component is FEXOFENADINE HYDROCHLORIDE.

MedlinePlus Drug Summary

Fexofenadine is used to relieve the allergy symptoms of seasonal allergic rhinitis (''hay fever''), including runny nose; sneezing; red, itchy, or watery eyes; or itching of the nose, throat, or roof of the mouth in adults and children 2 years of age and older. It is also used to relieve symptoms of urticaria (hives; red, itchy raised areas of the skin), including itching and rash in adults and children 6 months of age and older. Fexofenadine is in a class of medications called antihistamines. It works by blocking the effects of histamine, a substance in the body that causes allergy symptoms.

Related Packages: 70010-0183-03
Last Updated: 05/05/2024
MedLinePlus Full Drug Details: Fexofenadine

Product Information

NDC	70010-0183
Product ID	70010-183_fa30c8ce-ad9e-b6fe-e053-6294a90a2443
Associated GPIs
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
Proprietary Name	Fexofenadine HCL
Proprietary Name Suffix	n/a
Non-Proprietary Name	Fexofenadine HCL
Product Type	HUMAN OTC DRUG
Dosage Form	TABLET
Route	ORAL
Active Ingredient Strength	180
Active Ingredient Units	mg/1
Substance Name	FEXOFENADINE HYDROCHLORIDE
Labeler Name	GRANULES PHARMACEUTICALS INC.
Pharmaceutical Class	Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
DEA Schedule	n/a
Marketing Category	ANDA
Application Number	ANDA211075
Listing Certified Through	2024-12-31

Package

NDC 70010-0183-03 (70010018303)

Pricing Information	N/A
NDC Package Code	70010-183-03
Billing NDC	70010018303
Package	30 TABLET in 1 BOTTLE (70010-183-03)
Marketing Start Date	2023-04-25
NDC Exclude Flag	N