Alendronate Sodium
- Product NDC
- 68071-1514
- 11-digit product format
- 680711514
- Labeler code
- 68071
- Product ID
- 68071-1514_bb04f3ce-396e-5871-e053-2a95a90aaf14
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Alendronate Sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA090124
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-1514-4 | 68071151404 | 4 TABLET in 1 BOX (68071-1514-4) | 4 tablet | 2019-05-23 | 0000-00-00 | No | No | Current |