Details for New Drug Application (NDA): 209177
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The generic ingredient in PROMETHAZINE HYDROCHLORIDE is codeine phosphate; phenylephrine hydrochloride; promethazine hydrochloride. There are nineteen drug master file entries for this compound. Two suppliers are listed for this compound. Additional details are available on the codeine phosphate; phenylephrine hydrochloride; promethazine hydrochloride profile page.
Summary for 209177
Tradename: | PROMETHAZINE HYDROCHLORIDE |
Applicant: | Strides Pharma |
Ingredient: | promethazine hydrochloride |
Patents: | 0 |
Suppliers and Packaging for NDA: 209177
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
PROMETHAZINE HYDROCHLORIDE | promethazine hydrochloride | TABLET;ORAL | 209177 | ANDA | Strides Pharma Science Limited | 64380-792 | 64380-792-06 | 100 TABLET in 1 BOTTLE, PLASTIC (64380-792-06) |
PROMETHAZINE HYDROCHLORIDE | promethazine hydrochloride | TABLET;ORAL | 209177 | ANDA | Strides Pharma Science Limited | 64380-792 | 64380-792-08 | 1000 TABLET in 1 BOTTLE, PLASTIC (64380-792-08) |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 12.5MG | ||||
Approval Date: | Jun 30, 2017 | TE: | AB | RLD: | No |
Profile for product number 002
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 25MG | ||||
Approval Date: | Jun 30, 2017 | TE: | AB | RLD: | No |
Profile for product number 003
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 50MG | ||||
Approval Date: | Jun 30, 2017 | TE: | AB | RLD: | No |
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