Product NDC: | 0378-3288 |
Proprietary Name: | Etidronate Disodium |
Non Proprietary Name: | etidronate disodium |
Active Ingredient(s): | 400 mg/1 & nbsp; etidronate disodium |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0378-3288 |
Labeler Name: | Mylan Pharmaceuticals Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA075800 |
Marketing Category: | ANDA |
Start Marketing Date: | 20120507 |
Package NDC: | 0378-3288-91 |
Package Description: | 60 TABLET in 1 BOTTLE, PLASTIC (0378-3288-91) |
NDC Code | 0378-3288-91 |
Proprietary Name | Etidronate Disodium |
Package Description | 60 TABLET in 1 BOTTLE, PLASTIC (0378-3288-91) |
Product NDC | 0378-3288 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | etidronate disodium |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20120507 |
Marketing Category Name | ANDA |
Labeler Name | Mylan Pharmaceuticals Inc. |
Substance Name | ETIDRONATE DISODIUM |
Strength Number | 400 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Bisphosphonate [EPC],Diphosphonates [Chemical/Ingredient] |