Package 81033-016-50

Brand: promethazine hydrochloride

Generic: promethazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 81033-016-50
Digits Only 8103301650
Product NDC 81033-016
Product ID 81033-016_303b389f-b276-52cb-e063-6294a90a6e2e
Description

50 CUP, UNIT-DOSE in 1 CARTON (81033-016-50) / 5 mL in 1 CUP, UNIT-DOSE (81033-016-05)

Marketing

Marketing Status
Marketed Since 2024-12-31
Brand promethazine hydrochloride
Generic promethazine hydrochloride
Sample Package No

Linked Drug Pages (1)

PROMETHAZINE HYDROCHLORIDE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "303b389f-b276-52cb-e063-6294a90a6e2e", "openfda": {"unii": ["R61ZEH7I1I"], "rxcui": ["992432"], "spl_set_id": ["28793bd2-bd40-4571-e063-6394a90ae789"], "manufacturer_name": ["Kesin Pharma Corporation"]}, "finished": true, "packaging": [{"sample": false, "description": "50 CUP, UNIT-DOSE in 1 CARTON (81033-016-50)  / 5 mL in 1 CUP, UNIT-DOSE (81033-016-05)", "package_ndc": "81033-016-50", "marketing_start_date": "20241231"}], "brand_name": "PROMETHAZINE HYDROCHLORIDE", "product_id": "81033-016_303b389f-b276-52cb-e063-6294a90a6e2e", "dosage_form": "SOLUTION", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "81033-016", "generic_name": "PROMETHAZINE HYDROCHLORIDE", "labeler_name": "Kesin Pharma Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PROMETHAZINE HYDROCHLORIDE", "active_ingredients": [{"name": "PROMETHAZINE HYDROCHLORIDE", "strength": "6.25 mg/5mL"}], "application_number": "ANDA040891", "marketing_category": "ANDA", "marketing_start_date": "20241231", "listing_expiration_date": "20261231"}