promethazine hydrochloride
Generic: promethazine hydrochloride
Labeler: pd-rx pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
promethazine hydrochloride
Generic Name
promethazine hydrochloride
Labeler
pd-rx pharmaceuticals, inc.
Dosage Form
TABLET
Routes
Active Ingredients
promethazine hydrochloride 50 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
43063-447
Product ID
43063-447_2b25624a-3d1a-c6b4-e063-6394a90a4b75
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA091179
Listing Expiration
2026-12-31
Marketing Start
2011-03-03
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
43063447
Hyphenated Format
43063-447
Supplemental Identifiers
RxCUI
UPC
UNII
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
ANDA091179 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 50 mg/1
Packaging
- 4 TABLET in 1 BOTTLE, PLASTIC (43063-447-04)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2b25624a-3d1a-c6b4-e063-6394a90a4b75", "openfda": {"upc": ["0343063447048"], "unii": ["R61ZEH7I1I"], "rxcui": ["992475"], "spl_set_id": ["12400c65-f93b-47a5-8167-1fb14337130b"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "4 TABLET in 1 BOTTLE, PLASTIC (43063-447-04)", "package_ndc": "43063-447-04", "marketing_start_date": "20120221"}], "brand_name": "Promethazine Hydrochloride", "product_id": "43063-447_2b25624a-3d1a-c6b4-e063-6394a90a4b75", "dosage_form": "TABLET", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "43063-447", "generic_name": "Promethazine Hydrochloride", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Promethazine Hydrochloride", "active_ingredients": [{"name": "PROMETHAZINE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA091179", "marketing_category": "ANDA", "marketing_start_date": "20110303", "listing_expiration_date": "20261231"}