Package 68071-4544-2

Brand: promethazine hydrochloride

Generic: promethazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68071-4544-2
Digits Only 6807145442
Product NDC 68071-4544
Product ID 68071-4544_2dd17384-f3a5-70d3-e063-6294a90aeb7f
Description

12 TABLET in 1 BOTTLE (68071-4544-2)

Marketing

Marketing Status
Discontinued 2026-12-31
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": "2dd17384-f3a5-70d3-e063-6294a90aeb7f", "openfda": {"upc": ["0368071454420"], "unii": ["R61ZEH7I1I"], "rxcui": ["992447"], "spl_set_id": ["74834e1b-0d90-0542-e053-2991aa0aa1ef"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "12 TABLET in 1 BOTTLE (68071-4544-2)", "package_ndc": "68071-4544-2", "marketing_end_date": "20261231", "marketing_start_date": "20180828"}], "brand_name": "Promethazine Hydrochloride", "product_id": "68071-4544_2dd17384-f3a5-70d3-e063-6294a90aeb7f", "dosage_form": "TABLET", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "68071-4544", "generic_name": "Promethazine Hydrochloride", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Promethazine Hydrochloride", "active_ingredients": [{"name": "PROMETHAZINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA083426", "marketing_category": "ANDA", "marketing_end_date": "20261231", "marketing_start_date": "19730919"}