NDC 68071-3771 – Alendronate Sodium

Alendronate Sodium 70 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68071-3771

Product details

Brand name
Alendronate Sodium
Generic name
Alendronate sodium
Labeler
NuCare Pharmaceuticals, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA076768
Marketed since
August 4, 2008
Listing expires
December 31, 2026
Pharmacologic class
Bisphosphonate

Active ingredients

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

Package NDC codes (1)

Package NDCDescriptionSince
68071-3771-515 BLISTER PACK in 1 CARTON (68071-3771-5) / 1 TABLET in 1 BLISTER PACKJan 14, 2025

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