Package 68084-155-01
Brand: promethazine hydrochloride
Generic: promethazine hydrochloridePackage Facts
Identity
Package NDC
68084-155-01
Digits Only
6808415501
Product NDC
68084-155
Description
100 BLISTER PACK in 1 CARTON (68084-155-01) / 1 TABLET in 1 BLISTER PACK (68084-155-11)
Marketing
Marketing Status
Brand
promethazine hydrochloride
Generic
promethazine hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "437dac5e-3b6a-4c85-e063-6394a90a0d43", "openfda": {"unii": ["R61ZEH7I1I"], "rxcui": ["992447"], "spl_set_id": ["a8fe4bc5-961b-4441-b8e2-ef93e4e137b6"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (68084-155-01) / 1 TABLET in 1 BLISTER PACK (68084-155-11)", "package_ndc": "68084-155-01", "marketing_start_date": "20060830"}], "brand_name": "Promethazine Hydrochloride", "product_id": "68084-155_437dac5e-3b6a-4c85-e063-6394a90a0d43", "dosage_form": "TABLET", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "68084-155", "generic_name": "Promethazine Hydrochloride", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Promethazine Hydrochloride", "active_ingredients": [{"name": "PROMETHAZINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA040596", "marketing_category": "ANDA", "marketing_start_date": "20060830", "listing_expiration_date": "20261231"}