Alendronate Sodium
- Product NDC
- 0378-3566
- 11-digit product format
- 003783566
- Labeler code
- 0378
- Product ID
- 0378-3566_0e69141b-bacf-4224-a4ea-1c233551f852
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- alendronate sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Mylan Pharmaceuticals Inc
- Application
- ANDA076584
- Marketing category
- ANDA
- Marketing start
- 2008-08-04
- Marketing end
- 2019-03-31
- Substance
- ALENDRONATE SOD
- Active strength
- 5 mg/1
- Pharmacologic classes
- Bisphosphonate
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record