Alendronate
- Product NDC
- 68071-4072
- 11-digit product format
- 680714072
- Labeler code
- 68071
- Product ID
- 68071-4072_58106fd7-d266-3fe9-e053-2a91aa0ade1a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ALENDRONATE SODIUM
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA090258
- Marketing category
- ANDA
- Marketing start
- 2015-09-30
- 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