Alendronate Sodium
- Product NDC
- 33261-820
- 11-digit product format
- 332610820
- Labeler code
- 33261
- Product ID
- 33261-820_353a5ff7-34d8-4cb4-aaab-1cba7ed4b4de
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Alendronate Sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Aidarex Pharmaceuticals LLC
- Application
- ANDA075710
- Marketing category
- ANDA
- Marketing start
- 2008-02-06
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 33261-820-01 | Alendronate Sodium | 20 in 1 PACKET | TABLET | 20 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 33261-820 | ALENDRONATE SODIUM TABLET [AIDAREX PHARMACEUTICALS LLC] | 5 | Legacy NDC, 1 package rows | 20140331_2f5d8719-d7b1-4f8f-8315-8b8e59798175.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 33261-820-01 | 33261082001 | 20 in 1 PACKET | Historical |