Alendronate Sodium
- Product NDC
- 50090-2322
- 11-digit product format
- 500902322
- Labeler code
- 50090
- Product ID
- 50090-2322_9f53d8ef-abfc-425c-abae-1a284c649e8d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Alendronate Sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- 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#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-2322 | ALENDRONATE SODIUM TABLET [A-S MEDICATION SOLUTIONS] | 14 | Legacy NDC | 20230208_70c27a96-70b1-4d2a-959b-89361fd20c37.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-2322-0 | 50090232200 | 1 BLISTER PACK in 1 CARTON (50090-2322-0) > 4 TABLET in 1 BLISTER PACK | 1 blister pack | 2016-03-02 | 0000-00-00 | No | No | Current |
| 50090-2322-1 | 50090232201 | 1 BLISTER PACK in 1 CARTON (50090-2322-1) > 12 TABLET in 1 BLISTER PACK | 1 blister pack | 2016-03-02 | 0000-00-00 | No | No | Current |