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DIDRONEL
DIDRONEL - 0149-0406-60 - (ETIDRONATE DISODIUM)
Drug Information of DIDRONEL
| Product NDC: | 0149-0406 |
| Proprietary Name: | DIDRONEL |
| 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) |
Labeler Information of DIDRONEL
| Product NDC: | 0149-0406 |
| Labeler Name: | Procter & Gamble Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA017831 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19830812 |
Package Information of DIDRONEL
| Package NDC: | 0149-0406-60 |
| Package Description: | 60 TABLET in 1 BOTTLE (0149-0406-60) |
NDC Information of DIDRONEL
| NDC Code | 0149-0406-60 |
| Proprietary Name | DIDRONEL |
| Package Description | 60 TABLET in 1 BOTTLE (0149-0406-60) |
| Product NDC | 0149-0406 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | ETIDRONATE DISODIUM |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19830812 |
| Marketing Category Name | NDA |
| Labeler Name | Procter & Gamble Pharmaceuticals, Inc. |
| Substance Name | ETIDRONATE DISODIUM |
| Strength Number | 400 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Bisphosphonate [EPC],Diphosphonates [Chemical/Ingredient] |
