promethazine hydrochloride
Generic: promethazine hydrochloride
Labeler: hikma pharmaceuticals usa inc.Drug Facts
Product Profile
Brand Name
promethazine hydrochloride
Generic Name
promethazine hydrochloride
Labeler
hikma pharmaceuticals usa inc.
Dosage Form
INJECTION
Routes
Active Ingredients
promethazine hydrochloride 50 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
0641-0956
Product ID
0641-0956_69363376-bd70-47d7-ad97-39b3772728fa
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA083312
Listing Expiration
2026-12-31
Marketing Start
1973-09-19
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
06410956
Hyphenated Format
0641-0956
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
promethazine hydrochloride (source: ndc)
Generic Name
promethazine hydrochloride (source: ndc)
Application Number
ANDA083312 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 50 mg/mL
Packaging
- 25 VIAL in 1 CARTON (0641-0956-25) / 1 mL in 1 VIAL (0641-0956-21)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR"], "spl_id": "69363376-bd70-47d7-ad97-39b3772728fa", "openfda": {"unii": ["R61ZEH7I1I"], "rxcui": ["992460", "992858"], "spl_set_id": ["365138a6-28d8-4881-a3e9-02c80aaf83e8"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (0641-0956-25) / 1 mL in 1 VIAL (0641-0956-21)", "package_ndc": "0641-0956-25", "marketing_start_date": "19730919"}], "brand_name": "Promethazine Hydrochloride", "product_id": "0641-0956_69363376-bd70-47d7-ad97-39b3772728fa", "dosage_form": "INJECTION", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "0641-0956", "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"}