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For this drug, our server compiled this detailed Chemical Profile.
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Click the Chemical Profile link above for detailed information.
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FDA Approval Activities for this Drug
Alendronate Sodium Tablets, 35 & 70 mg, Barr, ANDA 76-184 4/23/02
Alendronate Sodium Tablets, 5, 10 & 40 mg, Ivax ANDA 75-711 7/24/02
Alendronate Sodium Tablets, 5, 10, 35, 40 & 70 mg (base), Teva ANDA 75-710 Fosamax (alendronate sodium) Solution, Merck NDA 21-575 9/17/03 9/25/03 9/25/03
Fosamax (alendronate sodium) Tablets, Merck & Co., NDA 20-560/S-037 3/24/03 3/26/03
Fosamax (alendronate sodium) Tablets, Merck & Co., NDA 20-560/S-036 8/5/02 8/12/02 8/5/02
Fosamax (alendronate sodium) Tablets, Merck & Co., NDA 20-560/S-033 8/13/02 8/14/02
Fosamax (alendronate sodium) Tablets, Merck & Co., NDA 20-560/S-031 7/25/02 7/26/02
Fosamax (alendronate sodium) Tablets, Merck & Co., NDA 20-560/S-028 9/16/02 9/20/02 9/17/02
Fosamax Tablets,10mg, Merck Research NDA 20-560/S-012 6/16/99 6/17/99 6/17/99 6/19/00
Fosamax Indication: for the treatment of glucocorticoid-induced osteoporosis in men and women receiving glucocorticoids in a daily dosage equivalent to 7.5 mg or greater of prednisone and who have low bone mineral density.
Fosamax Tablets, 5mg, 10mg & 40 mg, Merck Research NDA 20-560/S-013 6/8/99 6/19/00
Fosamax (alendronate sodium) Tablets,10mg, Merck Research NDA 20-560/S-018 11/24/99 12/29/99 4/24/03
Fosamax (alendronate sodium) Tablets,10mg, Merck Research NDA 20-560/S-015 11/24/99 12/29/99 4/24/03
Fosamax (alendronate sodium) Tablets,35 & 70mg, Merck Research NDA 20-560/S-021 & S-22 10/20/00 10/30/00 8/16/01
Fosamax Indication: for the prevention (S-021) and treatment (S-022) of postmenopausal osteoporosis, respectively.
Fosamax (alendronate sodium) Tablets,10mg, Merck Research NDA 20-560/S-023 9/29/00 10/10/00
Fosamax Indication: Treatment to increase bone mass in men with osteoporosis.
Fosamax (alendronate sodium) Tablets,70mg, Merck & Co., NDA 20-560/S-024 & S-025 1/31/01 2/8/01 2/8/01
Fosamax (alendronate sodium) Tablets, Merck & Co., NDA 20-560/S40 9/17/03 9/29/03
Fosamax Indication: Treatment to increase bone mass in men with osteoporosis. Alendronate Sodium Tablets, Mylan Pharmaceuticals, Fosamax (alendronate sodium) Tablets & Oral Solution, Merck Fosamax (alendronate sodium) Tablets & Oral Solution, Merck Fosamax (alendronate sodium) Tablets & Oral Solution, Merck Alendronate Sodium Tablets, Watson Laboratories | Fosamax Plus D (alendronate sodium vitamin D3) Tablets, Merck & Co., Approval | Fosamax (alendronate sodium) Tablets, Merck & Co., Labeling Revision | Fosamax (alendronate sodium) Oral Solution, Merck & Co., Labeling Revision | Fosamax Plus D (alendronate sodium Vitamin D3) Tablets, Merck & Co., Labeling Revsion | Fosamax (alendronate sodium) Tablets, Merck & Co., New or Modified Indication | Fosamax (alendronate sodium) Oral Solution, Merck & Co., Labeling Revision | Fosamax (alendronate sodium) Tablets, Merck & Co., Labeling Revision | Fosamax Plus D (alendronate sodium I.U. Vitamin D) Tablets, Merck & Co., Labeling Revision
Visit Betterchem's Drug Index for FDA's latest approval information.
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