Alendronate Sodium
- Product NDC
- 51224-301
- 11-digit product format
- 512240301
- Labeler code
- 51224
- Product ID
- 51224-301_640b0622-236e-46bd-8b46-1b1083719826
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Alendronate Sodium
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- TAGI Pharma, Inc.
- Application
- ANDA090520
- Marketing category
- ANDA
- Marketing start
- 2013-02-25
- Marketing end
- 2022-04-30
- Substance
- ALENDRONATE SODIUM
- Active strength
- 70 mg/75mL
- Pharmacologic classes
- Bisphosphonate [EPC],Diphosphonates [CS]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 51224-301-10 | 51224030110 | 4 BOTTLE, UNIT-DOSE in 1 CARTON (51224-301-10) > 75 mL in 1 BOTTLE, UNIT-DOSE | 2013-02-25 | 2022-04-30 | No | No | Current |