Once Weekly Alendronate Sodium Tablets, Usp 70 Mg

US $150

  • San Francisco, California, United States
  • Jan 30th
2 packages of 12 tablets each. By Sun Pharma Global Inc. | Last revised: 3 July 2013 Distributed by: Caraco Pharmaceutical Laboratories, Ltd.  1150 Elijah McCoy Drive, Detroit, MI 48202 Manufactured by: Sun Pharmaceutical Ind. Ltd.  Halol-Baroda Highway, Halol-389 350, Gujarat, India. ISS. 12/2012 PJPI0339C PRINCIPAL DISPLAY PANEL-carton-70mg NDC 41616-638-68  Once Weekly  Alendronate Sodium Tablets, USP 70 mg  Rx only  4 TABLETS  SUN PHARMACEUTICAL INDUSTRIES LTD.PHARMACIST: Dispense the Medication Guide provided separately to each patient ALENDRONATE SODIUM alendronate sodium tablet Product Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:41616-638 Route of Administration ORAL DEA Schedule Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALENDRONATE SODIUM (ALENDRONIC ACID) ALENDRONIC ACID 70 mg Inactive Ingredients Ingredient Name Strength CELLULOSE, MICROCRYSTALLINE STARCH, CORN SILICON DIOXIDE MAGNESIUM STEARATE Product Characteristics Color WHITE (White to Off-white) Score no score Shape ROUND Size 11mm Flavor Imprint Code 638 Contains Packaging # Item Code Package Description Multilevel Packaging 1 NDC:41616-638-68 1 BLISTER PACK in 1 CARTON contains a BLISTER PACK 1 4 TABLET in 1 BLISTER PACK This package is contained within the CARTON (41616-638-68) Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA090022 09/10/2008 Labeler — Sun Pharma Global Inc. (865367643) Establishment Name Address ID/FEI Operations Sun Pharmaceutical Industries Limited 725959238 MANUFACTURE (41616-635), ANALYSIS (41616-635)

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