APO ALE35 Pill — WHITE OVAL, 10mm — Alendronate
| Imprint | APO / ALE35 |
|---|---|
| Colour | WHITE |
| Shape | OVAL |
| Size | 10 |
| Strength | ALENDRONATE SODIUM 35 mg |
| Dosage form | Tablet |
| Manufacturer | Apotex Corp. |
| NDC | 60505-2594 |
| Schedule | — |
| Availability | — |
| Ingredients | ALENDRONATE SODIUM[ALENDRONIC ACID] |
What does this imprint mean?
The imprint "APO ALE35" is a code stamped or printed on the tablet or capsule by the manufacturer, used to identify the drug, its strength and the maker.
Active ingredient
Alendronate
Uses and warnings
No boxed warning. Key warnings: "Upper gastrointestinal adverse reactions can occur" - patients must follow strict dosing instructions (full glass of water, remain upright at least 30 minutes); "hypocalcemia" must be corrected before starting therapy; "severe bone, joint, or muscle pain" may occur, with discontinuation considered if severe; "osteonecrosis of the jaw has been reported," generally in cancer patients or those with risk factors; and "atypical fractures, including femoral fractures," have been reported with long-term bisphosphonate use.
Indicated for "treatment and prevention of osteoporosis in postmenopausal women," to "increase bone mass in men with osteoporosis," for "treatment of glucocorticoid-induced osteoporosis," and for "treatment of Paget's disease of bone." The label notes that for patients at low risk of fracture, clinicians should "consider drug discontinuation after 3 to 5 years of use."
How to identify this pill
- • Check the imprint matches exactly: "APO ALE35".
- • Confirm the colour (WHITE) and shape (OVAL).
- • Compare the size (10) against a ruler if possible.
- • When in doubt, confirm with a pharmacist before taking any medication.
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Official references
Source: FDA Structured Product Label via NLM Pillbox archive (retired 2021); source file 93655dd1-1a4c-6697-e899-5211039379ca.xml