Details for New Drug Application (NDA): 212779
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The generic ingredient in POTASSIUM CITRATE is potassium citrate. There are two hundred and forty drug master file entries for this compound. Seventeen suppliers are listed for this compound. Additional details are available on the potassium citrate profile page.
Summary for 212779
Tradename: | POTASSIUM CITRATE |
Applicant: | Ani Pharms |
Ingredient: | potassium citrate |
Patents: | 0 |
Pharmacology for NDA: 212779
Mechanism of Action | Acidifying Activity Calcium Chelating Activity |
Physiological Effect | Decreased Coagulation Factor Activity |
Medical Subject Heading (MeSH) Categories for 212779
Suppliers and Packaging for NDA: 212779
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
POTASSIUM CITRATE | potassium citrate | TABLET, EXTENDED RELEASE;ORAL | 212779 | ANDA | ANI Pharmaceuticals, Inc. | 62559-291 | 62559-291-01 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (62559-291-01) |
POTASSIUM CITRATE | potassium citrate | TABLET, EXTENDED RELEASE;ORAL | 212779 | ANDA | ANI Pharmaceuticals, Inc. | 62559-292 | 62559-292-01 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (62559-292-01) |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET, EXTENDED RELEASE;ORAL | Strength | 10MEQ | ||||
Approval Date: | Jan 14, 2020 | TE: | AB | RLD: | No |
Profile for product number 002
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET, EXTENDED RELEASE;ORAL | Strength | 15MEQ | ||||
Approval Date: | Jan 14, 2020 | TE: | AB | RLD: | No |
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