Package 0641-0949-35

Brand: promethazine hydrochloride

Generic: promethazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0641-0949-35
Digits Only 0641094935
Product NDC 0641-0949
Product ID 0641-0949_9b956a99-5a3c-4932-9d4e-804bbea8cee4
Description

25 AMPULE in 1 CARTON (0641-0949-35) / 1 mL in 1 AMPULE (0641-0949-31)

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": "9b956a99-5a3c-4932-9d4e-804bbea8cee4", "openfda": {"unii": ["R61ZEH7I1I"], "rxcui": ["992460", "992858"], "spl_set_id": ["d545105f-27dc-4820-b0b1-fcf17e0be0f0"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 AMPULE in 1 CARTON (0641-0949-35)  / 1 mL in 1 AMPULE (0641-0949-31)", "package_ndc": "0641-0949-35", "marketing_start_date": "19730919"}], "brand_name": "Promethazine Hydrochloride", "product_id": "0641-0949_9b956a99-5a3c-4932-9d4e-804bbea8cee4", "dosage_form": "INJECTION", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "0641-0949", "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"}