Details for New Drug Application (NDA): 214827
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The generic ingredient in CHLORPROMAZINE HYDROCHLORIDE is chlorpromazine hydrochloride. There are twenty-four drug master file entries for this compound. Twenty-nine suppliers are listed for this compound. Additional details are available on the chlorpromazine hydrochloride profile page.
Summary for 214827
Tradename: | CHLORPROMAZINE HYDROCHLORIDE |
Applicant: | Msn |
Ingredient: | chlorpromazine hydrochloride |
Patents: | 0 |
Suppliers and Packaging for NDA: 214827
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
CHLORPROMAZINE HYDROCHLORIDE | chlorpromazine hydrochloride | TABLET;ORAL | 214827 | ANDA | REMEDYREPACK INC. | 70518-3510 | 70518-3510-0 | 30 TABLET, SUGAR COATED in 1 BLISTER PACK (70518-3510-0) |
CHLORPROMAZINE HYDROCHLORIDE | chlorpromazine hydrochloride | TABLET;ORAL | 214827 | ANDA | REMEDYREPACK INC. | 70518-3510 | 70518-3510-1 | 100 POUCH in 1 BOX (70518-3510-1) / 1 TABLET, SUGAR COATED in 1 POUCH (70518-3510-2) |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 25MG | ||||
Approval Date: | Jan 27, 2022 | TE: | AB | RLD: | No |
Profile for product number 002
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 50MG | ||||
Approval Date: | Jan 27, 2022 | TE: | AB | RLD: | No |
Profile for product number 003
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 100MG | ||||
Approval Date: | Jan 27, 2022 | TE: | AB | RLD: | No |
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