NDC 65862-328 – Alendronate Sodium

Alendronate Sodium 35 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC65862-328

Product details

Brand name
Alendronate Sodium
Generic name
Alendronate Sodium
Labeler
Aurobindo Pharma Limited
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 (4)

Package NDCDescriptionSince
65862-328-041 BLISTER PACK in 1 CARTON (65862-328-04) / 4 TABLET in 1 BLISTER PACKAug 4, 2008
65862-328-083 BLISTER PACK in 1 CARTON (65862-328-08) / 4 TABLET in 1 BLISTER PACKAug 4, 2008
65862-328-1010 BLISTER PACK in 1 CARTON (65862-328-10) / 10 TABLET in 1 BLISTER PACKAug 4, 2008
65862-328-205 BLISTER PACK in 1 CARTON (65862-328-20) / 4 TABLET in 1 BLISTER PACKAug 4, 2008

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