Details for New Drug Application (NDA): 209755
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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-eight suppliers are listed for this compound. Additional details are available on the chlorpromazine hydrochloride profile page.
Summary for 209755
Tradename: | CHLORPROMAZINE HYDROCHLORIDE |
Applicant: | Amneal Pharms Co |
Ingredient: | chlorpromazine hydrochloride |
Patents: | 0 |
Suppliers and Packaging for NDA: 209755
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
CHLORPROMAZINE HYDROCHLORIDE | chlorpromazine hydrochloride | TABLET;ORAL | 209755 | ANDA | AvPAK | 50268-162 | 50268-162-15 | 50 BLISTER PACK in 1 BOX (50268-162-15) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-162-11) |
CHLORPROMAZINE HYDROCHLORIDE | chlorpromazine hydrochloride | TABLET;ORAL | 209755 | ANDA | AvPAK | 50268-163 | 50268-163-15 | 50 BLISTER PACK in 1 BOX (50268-163-15) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-163-11) |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 10MG | ||||
Approval Date: | Sep 10, 2018 | TE: | AB | RLD: | No |
Profile for product number 002
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 25MG | ||||
Approval Date: | Sep 10, 2018 | TE: | AB | RLD: | No |
Profile for product number 003
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 50MG | ||||
Approval Date: | Sep 10, 2018 | TE: | AB | RLD: | No |
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