FDA
Alendronate Sodium
The FDA lists this product in 55 strengths and forms.
Composition
- Active ingredients
- ALENDRONATE SODIUM EQ 35MG BASE
Strengths and forms
The FDA lists each strength of a product separately; these pages share one label.
- ALENDRONATE SODIUM EQ 70MG BASE · TabletANDA077982-004 · Discontinued
- ALENDRONATE SODIUM EQ 10MG BASE · TabletANDA077982-002 · Discontinued
- ALENDRONATE SODIUM EQ 35MG BASE · TabletANDA077982-003 · Discontinued
- ALENDRONATE SODIUM EQ 5MG BASE · TabletANDA077982-001 · Discontinued
- ALENDRONATE SODIUM EQ 35MG BASE · TabletANDA090022-003 · Prescription
- ALENDRONATE SODIUM EQ 5MG BASE · TabletANDA090022-001 · Prescription
- ALENDRONATE SODIUM EQ 70MG BASE · TabletANDA090022-004 · Prescription
- ALENDRONATE SODIUM EQ 10MG BASE · TabletANDA090022-002 · Prescription
- ALENDRONATE SODIUM EQ 35MG BASE · TabletThis page
- ALENDRONATE SODIUM EQ 5MG BASE · TabletANDA076584-001 · Discontinued
- ALENDRONATE SODIUM EQ 70MG BASE · TabletANDA076584-004 · Discontinued
- ALENDRONATE SODIUM EQ 10MG BASE · Tablet
At a glance
- Brand name
- Alendronate Sodium
- Route
- Oral
- Dosage form
- Tablet
- Applicant
- Rising
- Status
- Discontinued
- FDA approval
- 4 Aug 2008
- Application
- ANDA076584-003