Details for New Drug Application (NDA): 206883
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The generic ingredient in SEVELAMER HYDROCHLORIDE is sevelamer hydrochloride. There are thirty-two drug master file entries for this compound. Eight 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 Ltd |
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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