NDCFind

Glipizide 71205-0041

Product NDC

71205-0041
Manufacturer
Proficient Rx Lp
Dosage Form
Tablet
Route
Oral
Product Type
Human Prescription Drug
Marketing Start
September 25, 2002
Listing Expires
December 31, 2026
Application
ANDA075795
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Active Ingredients

IngredientStrength
Glipizide5 mg/1

Drug Class

Sulfonylurea [EPC]Sulfonylurea Compounds [CS]Sulfonylurea [EPC]

Packaging Options(4)

30 TABLET in 1 BOTTLE (71205-041-30)

60 TABLET in 1 BOTTLE (71205-041-60)

180 TABLET in 1 BOTTLE (71205-041-78)

90 TABLET in 1 BOTTLE (71205-041-90)