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Moexipril Hydrochloride - Moexipril Hydrochloride

Navigation: NDC > Supplier starting with: T > TEVA PHARMACEUTICALS USA INC
Field Value
NDC Code: 0093-0017
Proprietary Name: Moexipril Hydrochloride
Suffix:
Non-Proprietary Name: Moexipril Hydrochloride
Dosage Form: TABLET, FILM COATED
Method: ORAL
Original Marketing Date: 08-05-2003
Category Name: ANDA
Application Number: ANDA076204
Labeler: TEVA PHARMACEUTICALS USA INC
Substance Name: MOEXIPRIL HYDROCHLORIDE
Active Numerator Strength: 7.5
Active Ingredient Unit: mg/1
Pharm Classes: Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA]
DEA Schedule: