Package 45802-759-30

Brand: promethazine hydrochloride

Generic: promethazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 45802-759-30
Digits Only 4580275930
Product NDC 45802-759
Description

12 BLISTER PACK in 1 CARTON (45802-759-30) / 1 SUPPOSITORY in 1 BLISTER PACK (45802-759-00)

Marketing

Marketing Status
Marketed Since 2006-05-17
Brand promethazine hydrochloride
Generic promethazine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["RECTAL"], "spl_id": "14ed3375-f9ec-40bf-8529-cafc44c46f28", "openfda": {"unii": ["R61ZEH7I1I"], "rxcui": ["992441", "992454"], "spl_set_id": ["047b9a7c-586b-4635-a63e-2c7ce9ec34e7"], "manufacturer_name": ["Padagis Israel Pharmaceuticals Ltd"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "12 BLISTER PACK in 1 CARTON (45802-759-30)  / 1 SUPPOSITORY in 1 BLISTER PACK (45802-759-00)", "package_ndc": "45802-759-30", "marketing_start_date": "20060517"}], "brand_name": "Promethazine Hydrochloride", "product_id": "45802-759_14ed3375-f9ec-40bf-8529-cafc44c46f28", "dosage_form": "SUPPOSITORY", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "45802-759", "generic_name": "Promethazine Hydrochloride", "labeler_name": "Padagis Israel Pharmaceuticals Ltd", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Promethazine Hydrochloride", "active_ingredients": [{"name": "PROMETHAZINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA040500", "marketing_category": "ANDA", "marketing_start_date": "20060517", "listing_expiration_date": "20261231"}