49884-425 : Aliskiren 300 mg Oral Tablet, Film Coated
| NDC: | 49884-425 |
| Labeler: | Par Pharmaceutical, Inc. |
| Product Type: | Human Prescription Drug |
| Drug Name: |  Aliskiren |
| Dosage Form: | Oral Tablet, Film Coated |
| Application #: | ANDA206665 |
| Rev. Date: |
Appearance:
| Markings: | E;591 |
| Shapes: |
Oval |
| Colors: |
 Brown |
| Size (mm): | 18 |
| 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:
- 49884-425-11: 30 TABLET, FILM COATED IN 1 BOTTLE (49884‑425‑11)
Active Ingredients:
- Aliskiren Hemifumarate
Dosage Strength:
- 300 mg
Inactive Ingredients:
- Calcium Stearate
- Silicon Dioxide
- Crospovidone, Unspecified
- Hypromellose 2910 (6 Mpa.s)
- Ferric Oxide Red
- Microcrystalline Cellulose
- Polyethylene Glycol 8000
- Talc
- Titanium Dioxide /
Pharmaceutical Classes:
- Renin Inhibitor [EPC]
- Renin Inhibitors [MoA]
Related Products:
Based on records with the same trade name.- 49884-424 Aliskiren 150 mg Oral Tablet, Film Coated by Par Pharmaceutical, Inc.
- 66993-141 Aliskiren 150 mg Oral Tablet, Film Coated by Prasco Laboratories
- 66993-142 Aliskiren 300 mg Oral Tablet, Film Coated by Prasco Laboratories
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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.