NDC 64980-342 – Alendronate Sodium

Alendronate Sodium 70 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC64980-342

Product details

Brand name
Alendronate Sodium
Generic name
Alendronate Sodium
Labeler
Rising Pharma Holdings, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA090124
Marketed since
August 4, 2008
Listing expires
December 31, 2027
Pharmacologic class
Bisphosphonate

Active ingredients

Uses, dosage, side effects and warnings for Alendronate Sodium →

Package NDC codes (3)

Package NDCDescriptionSince
64980-342-01100 TABLET in 1 BOTTLE (64980-342-01)Sep 30, 2024
64980-342-141 BLISTER PACK in 1 CARTON (64980-342-14) / 4 TABLET in 1 BLISTER PACKAug 4, 2008
64980-342-50500 TABLET in 1 BOTTLE (64980-342-50)Sep 30, 2024

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