0004-0186 : Boniva 150 mg Oral Tablet
| NDC: | 0004-0186 |
| Labeler: | Genentech, Inc. |
| Product Type: | Human Prescription Drug |
| Drug Name: |  Boniva |
| Dosage Form: | Oral Tablet, Film Coated |
| Application #: | NDA021455 |
| Rev. Date: |
Appearance:
| Markings: | BNVA;150 |
| Shapes: |
Oval |
| Colors: |
 White |
| Size (mm): | 14 |
| Segments: * | 1 |
* Segments = the number of equally sized pieces which the pill can be broken into. In this case, a value of 1 indicates a solid pill with no score lines. | |
NDC Package Codes:
- 0004-0186-82: 3 BLISTER PACK IN 1 BOX (0004‑0186‑82) > 1 TABLET, FILM COATED IN 1 BLISTER PACK
- 0004-0186-83: 1 BLISTER PACK IN 1 BOX (0004‑0186‑83) > 3 TABLET, FILM COATED IN 1 BLISTER PACK
- 0004-0186-98: 1 BLISTER PACK IN 1 BOX (0004‑0186‑98) > 1 TABLET, FILM COATED IN 1 BLISTER PACK
Active Ingredients:
- Ibandronate Sodium
Dosage Strength:
- 150 mg
Inactive Ingredients:
- Lactose Monohydrate
- Povidone K25
- Cellulose, Microcrystalline
- Crospovidone
- Stearic Acid
- Silicon Dioxide
- Water
- Hypromelloses
- Titanium Dioxide
- Talc
- Polyethylene Glycol 6000
Pharmaceutical Classes:
- Bisphosphonate [EPC]
- Diphosphonates [CS]
Related Products:
Based on records with the same trade name.- 0004-0191 Boniva 3 mg/3ml Intravenous Injection, Solution by Genentech, Inc.
- 54868-5322 Boniva 150 mg Oral Tablet by Physicians Total Care, Inc.
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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.