Package 0641-6208-25

Brand: promethazine hydrochloride

Generic: promethazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0641-6208-25
Digits Only 0641620825
Product NDC 0641-6208
Product ID 0641-6208_0d145884-8a66-4169-ad24-1e983a1c734e
Description

25 VIAL in 1 CARTON (0641-6208-25) / 1 mL in 1 VIAL (0641-6208-01)

Marketing

Marketing Status
Marketed Since 1973-09-19
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": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "0d145884-8a66-4169-ad24-1e983a1c734e", "openfda": {"unii": ["R61ZEH7I1I"], "rxcui": ["992460"], "spl_set_id": ["b0d5abba-6fae-4f3c-b990-dd9c83c7b5a9"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (0641-6208-25)  / 1 mL in 1 VIAL (0641-6208-01)", "package_ndc": "0641-6208-25", "marketing_start_date": "19730919"}], "brand_name": "Promethazine Hydrochloride", "product_id": "0641-6208_0d145884-8a66-4169-ad24-1e983a1c734e", "dosage_form": "INJECTION", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "0641-6208", "generic_name": "Promethazine Hydrochloride", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Promethazine Hydrochloride", "active_ingredients": [{"name": "PROMETHAZINE HYDROCHLORIDE", "strength": "25 mg/mL"}], "application_number": "ANDA083312", "marketing_category": "ANDA", "marketing_start_date": "19730919", "listing_expiration_date": "20261231"}