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ACTONEL
ACTONEL - 0149-0472-02 - (RISEDRONATE SODIUM)
Drug Information of ACTONEL
| Product NDC: | 0149-0472 |
| Proprietary Name: | ACTONEL |
| Non Proprietary Name: | RISEDRONATE SODIUM |
| Active Ingredient(s): | 35 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: | 0149-0472 |
| Labeler Name: | Warner Chilcott Pharmaceuticals Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020835 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20020517 |
Package Information of ACTONEL
| Package NDC: | 0149-0472-02 |
| Package Description: | 36 DOSE PACK in 1 CASE (0149-0472-02) > 1 TRAY in 1 DOSE PACK > 1 TABLET, FILM COATED in 1 TRAY |
NDC Information of ACTONEL
| NDC Code | 0149-0472-02 |
| Proprietary Name | ACTONEL |
| Package Description | 36 DOSE PACK in 1 CASE (0149-0472-02) > 1 TRAY in 1 DOSE PACK > 1 TABLET, FILM COATED in 1 TRAY |
| Product NDC | 0149-0472 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | RISEDRONATE SODIUM |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20020517 |
| Marketing Category Name | NDA |
| Labeler Name | Warner Chilcott Pharmaceuticals Inc. |
| Substance Name | RISEDRONATE SODIUM |
| Strength Number | 35 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Bisphosphonate [EPC],Diphosphonates [Chemical/Ingredient] |
