Package 0641-1496-35

Brand: promethazine hydrochloride

Generic: promethazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0641-1496-35
Digits Only 0641149635
Product NDC 0641-1496
Product ID 0641-1496_80a400d2-d293-4180-bfa7-7a8ce0734bc5
Description

25 AMPULE in 1 PACKAGE (0641-1496-35) / 1 mL in 1 AMPULE (0641-1496-31)

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"], "spl_id": "80a400d2-d293-4180-bfa7-7a8ce0734bc5", "openfda": {"unii": ["R61ZEH7I1I"], "rxcui": ["992460", "992858"], "spl_set_id": ["13d9e59d-eadb-41d5-9f47-9c11a6efb31c"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 AMPULE in 1 PACKAGE (0641-1496-35)  / 1 mL in 1 AMPULE (0641-1496-31)", "package_ndc": "0641-1496-35", "marketing_start_date": "19730919"}], "brand_name": "Promethazine Hydrochloride", "product_id": "0641-1496_80a400d2-d293-4180-bfa7-7a8ce0734bc5", "dosage_form": "INJECTION", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "0641-1496", "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": "50 mg/mL"}], "application_number": "ANDA083312", "marketing_category": "ANDA", "marketing_start_date": "19730919", "listing_expiration_date": "20261231"}