Details for New Drug Application (NDA): 207222
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The generic ingredient in CHLORTHALIDONE is chlorthalidone. There are twenty-one drug master file entries for this compound. Thirty-four suppliers are listed for this compound. Additional details are available on the chlorthalidone profile page.
Summary for 207222
Tradename: | CHLORTHALIDONE |
Applicant: | Umedica |
Ingredient: | chlorthalidone |
Patents: | 0 |
Formulation / Manufacturing: | see details |
Pharmacology for NDA: 207222
Physiological Effect | Increased Diuresis |
Medical Subject Heading (MeSH) Categories for 207222
Suppliers and Packaging for NDA: 207222
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
CHLORTHALIDONE | chlorthalidone | TABLET;ORAL | 207222 | ANDA | Northwind Pharmaceuticals | 51655-790 | 51655-790-26 | 90 TABLET in 1 BOTTLE, PLASTIC (51655-790-26) |
CHLORTHALIDONE | chlorthalidone | TABLET;ORAL | 207222 | ANDA | Northwind Pharmaceuticals | 51655-790 | 51655-790-52 | 30 TABLET in 1 BOTTLE, PLASTIC (51655-790-52) |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 25MG | ||||
Approval Date: | May 24, 2018 | TE: | AB | RLD: | No |
Profile for product number 002
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 50MG | ||||
Approval Date: | May 24, 2018 | TE: | AB | RLD: | No |
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