alendronate sodium
- Product NDC
- 63187-580
- 11-digit product format
- 631870580
- Labeler code
- 63187
- Product ID
- 63187-580_e49bf96e-af26-459e-ac3d-344e8bd87eed
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- alendronate sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA076984
- Marketing category
- ANDA
- Marketing start
- 2008-08-04
- Marketing end
- 0000-00-00
- Substance
- ALENDRONATE SODIUM
- Active strength
- 70 mg/1
- Pharmacologic classes
- Bisphosphonate [EPC],Diphosphonates [CS]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record