NDCFind

Quinapril 71205-0484

Product NDC

71205-0484
Manufacturer
Proficient Rx Lp
Dosage Form
Tablet
Route
Oral
Product Type
Human Prescription Drug
Marketing Start
November 10, 2017
Listing Expires
December 31, 2026
Application
ANDA205823
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Active Ingredients

IngredientStrength
Quinapril Hydrochloride10 mg/1

Drug Class

Angiotensin Converting Enzyme Inhibitor [EPC]Angiotensin-converting Enzyme Inhibitors [MoA]

Packaging Options(3)

30 TABLET in 1 BOTTLE (71205-484-30)

60 TABLET in 1 BOTTLE (71205-484-60)

90 TABLET in 1 BOTTLE (71205-484-90)