ACTONEL is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Warner Chilcott Pharmaceuticals Inc.. The primary component is Risedronate Sodium.
| Product ID | 0149-0472_05985725-417c-44f4-9e38-4fed7cdfdaad |
| NDC | 0149-0472 |
| Product Type | Human Prescription Drug |
| Proprietary Name | ACTONEL |
| Generic Name | Risedronate Sodium |
| Dosage Form | Tablet, Film Coated |
| Route of Administration | ORAL |
| Marketing Start Date | 2002-05-17 |
| Marketing Category | NDA / NDA |
| Application Number | NDA020835 |
| Labeler Name | Warner Chilcott Pharmaceuticals Inc. |
| Substance Name | RISEDRONATE SODIUM |
| Active Ingredient Strength | 35 mg/1 |
| Pharm Classes | Bisphosphonate [EPC],Diphosphonates [CS] |
| NDC Exclude Flag | E |
| Listing Certified Through | 2017-12-31 |
| Marketing Start Date | 2002-05-17 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | NDA |
| Application Number | NDA020835 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2002-05-17 |
| Inactivation Date | 2019-10-21 |
| Marketing Category | NDA |
| Application Number | NDA020835 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2009-10-29 |
| Inactivation Date | 2019-10-21 |
| Marketing Category | NDA |
| Application Number | NDA020835 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2002-05-17 |
| Inactivation Date | 2019-10-21 |
| Ingredient | Strength |
|---|---|
| RISEDRONATE SODIUM | 35 mg/1 |
| SPL SET ID: | 563c6d6d-56df-43a7-a7aa-709c5ea3cdbe |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 0149-0470 | ACTONEL | RISEDRONATE SODIUM |
| 0149-0471 | ACTONEL | RISEDRONATE SODIUM |
| 0149-0472 | ACTONEL | RISEDRONATE SODIUM |
| 0149-0478 | ACTONEL | RISEDRONATE SODIUM |
| 0430-0470 | Actonel | Risedronate Sodium |
| 0430-0471 | Actonel | Risedronate Sodium |
| 0430-0472 | Actonel | Risedronate Sodium |
| 0430-0478 | Actonel | Risedronate Sodium |
| 0093-3098 | Risedronate Sodium | Risedronate Sodium |
| 0093-3099 | Risedronate Sodium | Risedronate Sodium |
| 0093-3100 | Risedronate Sodium | Risedronate Sodium |
| 0093-7771 | Risedronate Sodium | Risedronate Sodium |
| 0378-4044 | Risedronate Sodium | risedronate sodium |
| 0378-4114 | Risedronate Sodium | risedronate sodium |
| 0378-4150 | Risedronate Sodium | risedronate sodium |
| 0378-4714 | Risedronate Sodium | risedronate sodium |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() ACTONEL 75237477 2215222 Live/Registered |
ALLERGAN PHARMACEUTICALS INTERNATIONAL L 1997-02-06 |
![]() ACTONEL 74603273 not registered Dead/Abandoned |
Procter & Gamble Company, The 1994-11-09 |
![]() ACTONEL 74010973 1608809 Dead/Cancelled |
NORWICH EATON PHARMACEUTICALS, INC. 1989-12-15 |
![]() ACTONEL 73768517 1560433 Dead/Cancelled |
NORWICH EATON PHARMACEUTICALS, INC. 1988-12-09 |