Package 87063-016-30

Brand: promethazine hydrochloride

Generic: promethazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 87063-016-30
Digits Only 8706301630
Product NDC 87063-016
Description

30 TABLET in 1 BOTTLE (87063-016-30)

Marketing

Marketing Status
Marketed Since 2025-10-17
Brand promethazine hydrochloride
Generic promethazine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "41a47d00-8acc-6eba-e063-6294a90ae752", "openfda": {"unii": ["R61ZEH7I1I"], "rxcui": ["992438", "992447", "992475"], "spl_set_id": ["4d30e587-6d59-4cf5-ab45-c7639f759df9"], "manufacturer_name": ["ASCLEMED USA INC."]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (87063-016-00)", "package_ndc": "87063-016-00", "marketing_start_date": "20251017"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (87063-016-01)", "package_ndc": "87063-016-01", "marketing_start_date": "20251017"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (87063-016-05)", "package_ndc": "87063-016-05", "marketing_start_date": "20251017"}, {"sample": false, "description": "10 TABLET in 1 BOTTLE (87063-016-10)", "package_ndc": "87063-016-10", "marketing_start_date": "20251017"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (87063-016-20)", "package_ndc": "87063-016-20", "marketing_start_date": "20251017"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (87063-016-30)", "package_ndc": "87063-016-30", "marketing_start_date": "20251017"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (87063-016-60)", "package_ndc": "87063-016-60", "marketing_start_date": "20251017"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (87063-016-90)", "package_ndc": "87063-016-90", "marketing_start_date": "20251017"}], "brand_name": "Promethazine Hydrochloride", "product_id": "87063-016_41a47d00-8acc-6eba-e063-6294a90ae752", "dosage_form": "TABLET", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "87063-016", "generic_name": "Promethazine Hydrochloride", "labeler_name": "ASCLEMED USA INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Promethazine Hydrochloride", "active_ingredients": [{"name": "PROMETHAZINE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA040596", "marketing_category": "ANDA", "marketing_start_date": "20051214", "listing_expiration_date": "20261231"}