70748-173 : Sevelamer Hydrochloride 800 mg Oral Tablet
NDC: | 70748-173 |
Labeler: | Lupin Pharmaceuticals, Inc. |
Product Type: | Human Prescription Drug |
Drug Name: | Sevelamer Hydrochloride |
Dosage Form: | Oral Tablet |
Application #: | ANDA213145 |
Rev. Date: |
NDC Package Codes:
- 70748-173-26: 180 TABLET IN 1 BOTTLE (70748‑173‑26)
Active Ingredients:
- Sevelamer Hydrochloride
Dosage Strength:
- 800 mg
Pharmaceutical Classes:
- Phosphate Binder [EPC]
- Phosphate Chelating Activity [MoA]
Related Products:
Based on records with the same trade name.- 70748-172 Sevelamer Hydrochloride 400 mg Oral Tablet by Lupin Pharmaceuticals, Inc.
- 0955-1048 Sevelamer Hydrochloride 800 mg Oral Tablet, Film Coated by Winthrop U.S.
- 33342-241 Sevelamer Hydrochloride 400 mg Oral Tablet, Film Coated by Macleods Pharmaceuticals Limited
- 33342-242 Sevelamer Hydrochloride 800 mg Oral Tablet, Film Coated by Macleods Pharmaceuticals Limited
- 59651-087 Sevelamer Hydrochloride 400 mg Oral Tablet, Film Coated by Aurobindo Pharma Limited
- 59651-088 Sevelamer Hydrochloride 800 mg Oral Tablet, Film Coated by Aurobindo Pharma Limited
- 60687-449 Sevelamer Hydrochloride 800 mg Oral Tablet, Film Coated by American Health Packaging
- 68462-446 Sevelamer Hydrochloride 400 mg Oral Tablet, Film Coated by Glenmark Pharmaceuticals Inc., USA
- 68462-447 Sevelamer Hydrochloride 800 mg Oral Tablet, Film Coated by Glenmark Pharmaceuticals Inc., USA
- 72603-148 Sevelamer Hydrochloride 800 mg Oral Tablet, Film Coated by Northstar Rxllc
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