NDC 60723-207 – Alendronate

Alendronate Sodium 35 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC60723-207

Product details

Brand name
Alendronate
Generic name
Alendronate Sodium
Labeler
Hangzhou Minsheng Binjiang Pharmaceutical Co., Ltd.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA090258
Marketed since
December 5, 2017
Listing expires
December 31, 2026
Pharmacologic class
Bisphosphonate

Active ingredients

Uses, dosage, side effects and warnings for Alendronate →

Package NDC codes (3)

Package NDCDescriptionSince
60723-207-311 BLISTER PACK in 1 CARTON (60723-207-31) / 4 TABLET in 1 BLISTER PACKDec 5, 2017
60723-207-323 BLISTER PACK in 1 CARTON (60723-207-32) / 4 TABLET in 1 BLISTER PACKDec 5, 2017
60723-207-332 BLISTER PACK in 1 CARTON (60723-207-33) / 10 TABLET in 1 BLISTER PACKDec 5, 2017

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