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Fexofenadine Hydrochloride - fexofenadine hydrochloride

Navigation: NDC > Supplier starting with: U > UDL LABORATORIES INC.
Field Value
NDC Code: 51079-548
Proprietary Name: Fexofenadine Hydrochloride
Suffix:
Non-Proprietary Name: fexofenadine hydrochloride
Dosage Form: TABLET, FILM COATED
Method: ORAL
Original Marketing Date: 07-10-2011
Category Name: ANDA
Application Number: ANDA077081
Labeler: UDL LABORATORIES INC.
Substance Name: FEXOFENADINE HYDROCHLORIDE
Active Numerator Strength: 180
Active Ingredient Unit: mg/1
Pharm Classes:
DEA Schedule: