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Actonel
Actonel - 0430-0470-15 - (RISEDRONATE SODIUM)
Drug Information of Actonel
| Product NDC: | 0430-0470 |
| Proprietary Name: | Actonel |
| Non Proprietary Name: | RISEDRONATE SODIUM |
| Active Ingredient(s): | 25.8; 4.2 mg/1; mg/1 & nbsp; RISEDRONATE SODIUM |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Actonel
| Product NDC: | 0430-0470 |
| Labeler Name: | Warner Chilcott (US), LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020835 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19980327 |
Package Information of Actonel
| Package NDC: | 0430-0470-15 |
| Package Description: | 12 BOTTLE in 1 CASE (0430-0470-15) > 30 TABLET, FILM COATED in 1 BOTTLE |
NDC Information of Actonel
| NDC Code | 0430-0470-15 |
| Proprietary Name | Actonel |
| Package Description | 12 BOTTLE in 1 CASE (0430-0470-15) > 30 TABLET, FILM COATED in 1 BOTTLE |
| Product NDC | 0430-0470 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | RISEDRONATE SODIUM |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 19980327 |
| Marketing Category Name | NDA |
| Labeler Name | Warner Chilcott (US), LLC |
| Substance Name | RISEDRONATE SODIUM HEMI-PENTAHYDRATE; RISEDRONATE SODIUM MONOHYDRATE |
| Strength Number | 25.8; 4.2 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Bisphosphonate [EPC],Diphosphonates [Chemical/Ingredient],Bisphosphonate [EPC],Diphosphonates [Chemical/Ingredient] |
