NDC 10135-718 – Alendronate

Alendronate Sodium 35 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC10135-718

Product details

Brand name
Alendronate
Generic name
Alendronate sodium tablet
Labeler
Marlex Pharmaceuticals, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA090258
Marketed since
December 1, 2020
Listing expires
December 31, 2026
Pharmacologic class
Bisphosphonate

Active ingredients

Uses, dosage, side effects and warnings for Alendronate →

Package NDC codes (2)

Package NDCDescriptionSince
10135-718-123 BLISTER PACK in 1 CARTON (10135-718-12) / 4 TABLET in 1 BLISTER PACKDec 1, 2020
10135-718-441 BLISTER PACK in 1 CARTON (10135-718-44) / 4 TABLET in 1 BLISTER PACKDec 1, 2020

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