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637 (Alendronate 35 mg)

Pill imprint 637 has been identified as Alendronate sodium 35 mg.

Alendronate is used in the treatment of prevention of osteoporosis; osteoporosis; paget's disease; aseptic necrosis and belongs to the drug class bisphosphonates. Risk cannot be ruled out during pregnancy. Alendronate 35 mg is not a controlled substance under the Controlled Substance Act (CSA).

Alendronate sodium 35 mg 637
Alendronate sodium 35 mg 637
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Alendronate sodium
Imprint:
637
Strength:
35 mg
Color:
White
Size:
8.00 mm
Shape:
Round
Availability:
Prescription only
Drug Class:
Bisphosphonates
Pregnancy Category:
C - Risk cannot be ruled out
CSA Schedule:
Not a controlled drug
Manufacturer:
Sun Pharmaceuticals
National Drug Code (NDC):
41616-0637
Inactive Ingredients:
microcrystalline cellulose
corn starch
silicon dioxide
magnesium stearate
Other Manufacturers / Repackagers:
NDC CodeManufacturer / Repackager
47335-0637 Sun Pharmaceutical Industries Inc.

Note: Inactive ingredients may vary.

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