Details for New Drug Application (NDA): 206883
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The generic ingredient in SEVELAMER HYDROCHLORIDE is sevelamer hydrochloride. There is one drug master file entry for this compound. Nine suppliers are listed for this compound. Additional details are available on the sevelamer hydrochloride profile page.
Summary for 206883
| Tradename: | SEVELAMER HYDROCHLORIDE |
| Applicant: | Macleods Pharms |
| Ingredient: | sevelamer hydrochloride |
| Patents: | 0 |
Pharmacology for NDA: 206883
| Mechanism of Action | Phosphate Chelating Activity |
Suppliers and Packaging for NDA: 206883
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| SEVELAMER HYDROCHLORIDE | sevelamer hydrochloride | TABLET;ORAL | 206883 | ANDA | Macleods Pharmaceuticals Limited | 33342-241 | 33342-241-65 | 360 TABLET, FILM COATED in 1 BOTTLE (33342-241-65) |
| SEVELAMER HYDROCHLORIDE | sevelamer hydrochloride | TABLET;ORAL | 206883 | ANDA | Macleods Pharmaceuticals Limited | 33342-242 | 33342-242-07 | 30 TABLET, FILM COATED in 1 BOTTLE (33342-242-07) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 400MG | ||||
| Approval Date: | May 26, 2023 | TE: | AB | RLD: | No | ||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 800MG | ||||
| Approval Date: | May 26, 2023 | TE: | AB | RLD: | No | ||||
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