Details for New Drug Application (NDA): 211627
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The generic ingredient in CHLORTHALIDONE is chlorthalidone. There are twenty-one drug master file entries for this compound. Thirty-five suppliers are listed for this compound. Additional details are available on the chlorthalidone profile page.
Summary for 211627
Tradename: | CHLORTHALIDONE |
Applicant: | Unichem |
Ingredient: | chlorthalidone |
Patents: | 0 |
Formulation / Manufacturing: | see details |
Pharmacology for NDA: 211627
Physiological Effect | Increased Diuresis |
Medical Subject Heading (MeSH) Categories for 211627
Suppliers and Packaging for NDA: 211627
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
CHLORTHALIDONE | chlorthalidone | TABLET;ORAL | 211627 | ANDA | Unichem Pharmaceuticals (USA), Inc. | 29300-333 | 29300-333-01 | 100 TABLET in 1 BOTTLE, PLASTIC (29300-333-01) |
CHLORTHALIDONE | chlorthalidone | TABLET;ORAL | 211627 | ANDA | Unichem Pharmaceuticals (USA), Inc. | 29300-333 | 29300-333-10 | 1000 TABLET in 1 BOTTLE, PLASTIC (29300-333-10) |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 25MG | ||||
Approval Date: | Aug 6, 2019 | TE: | AB | RLD: | No |
Profile for product number 002
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 50MG | ||||
Approval Date: | Aug 6, 2019 | TE: | AB | RLD: | No |
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