NDC 68788-7130 – Alendronate Sodium

Alendronate Sodium 70 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68788-7130

Product details

Brand name
Alendronate Sodium
Generic name
Alendronate sodium
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA076768
Marketed since
March 30, 2018
Listing expires
December 31, 2027
Pharmacologic class
Bisphosphonate

Active ingredients

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

Package NDC codes (1)

Package NDCDescriptionSince
68788-7130-44 TABLET in 1 BLISTER PACK (68788-7130-4)Mar 30, 2018

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