Glipizide 70518-2308

Product NDC

70518-2308

Manufacturer: Remedyrepack Inc.
Dosage Form: Tablet, Film Coated, Extended Release
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: September 11, 2019
Listing Expires: December 31, 2027
Application: ANDA204720

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Active Ingredients

Ingredient	Strength
Glipizide	2.5 mg/1

Drug Class

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

Packaging Options(2)

70518-2308-00

30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (70518-2308-0)

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70518-2308-01

90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-2308-1)

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