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promethazine hydrochloride and codeine phosphate - 57664-185-31 - (promethazine hydrochloride and codeine phosphate)

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Drug Information of promethazine hydrochloride and codeine phosphate

Product NDC: 57664-185
Proprietary Name: promethazine hydrochloride and codeine phosphate
Non Proprietary Name: promethazine hydrochloride and codeine phosphate
Active Ingredient(s): 10; 6.25    mg/5mL; mg/5mL & nbsp;   promethazine hydrochloride and codeine phosphate
Administration Route(s): ORAL
Dosage Form(s): SYRUP
Coding System: National Drug Codes(NDC)

Labeler Information of promethazine hydrochloride and codeine phosphate

Product NDC: 57664-185
Labeler Name: Caraco Pharmaceutical Laboratories, Ltd.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090180
Marketing Category: ANDA
Start Marketing Date: 20100317

Package Information of promethazine hydrochloride and codeine phosphate

Package NDC: 57664-185-31
Package Description: 118 mL in 1 BOTTLE (57664-185-31)

NDC Information of promethazine hydrochloride and codeine phosphate

NDC Code 57664-185-31
Proprietary Name promethazine hydrochloride and codeine phosphate
Package Description 118 mL in 1 BOTTLE (57664-185-31)
Product NDC 57664-185
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name promethazine hydrochloride and codeine phosphate
Dosage Form Name SYRUP
Route Name ORAL
Start Marketing Date 20100317
Marketing Category Name ANDA
Labeler Name Caraco Pharmaceutical Laboratories, Ltd.
Substance Name CODEINE PHOSPHATE; PROMETHAZINE HYDROCHLORIDE
Strength Number 10; 6.25
Strength Unit mg/5mL; mg/5mL
Pharmaceutical Classes Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient],Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of promethazine hydrochloride and codeine phosphate


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