promethazine hydrochloride
Generic: promethazine hydrochloride
Labeler: a-s medication solutionsDrug Facts
Product Profile
Brand Name
promethazine hydrochloride
Generic Name
promethazine hydrochloride
Labeler
a-s medication solutions
Dosage Form
TABLET
Routes
Active Ingredients
promethazine hydrochloride 25 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
50090-4608
Product ID
50090-4608_c3c1637d-7777-4709-8707-aa28fb86db9f
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA040712
Listing Expiration
2026-12-31
Marketing Start
2006-07-31
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
500904608
Hyphenated Format
50090-4608
Supplemental Identifiers
RxCUI
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
ANDA040712 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 25 mg/1
Packaging
- 90 TABLET in 1 BOTTLE (50090-4608-0)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "c3c1637d-7777-4709-8707-aa28fb86db9f", "openfda": {"unii": ["R61ZEH7I1I"], "rxcui": ["992447"], "spl_set_id": ["b54439a3-1d01-4c5f-8508-731790ae215b"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-4608-0)", "package_ndc": "50090-4608-0", "marketing_start_date": "20191015"}], "brand_name": "PROMETHAZINE HYDROCHLORIDE", "product_id": "50090-4608_c3c1637d-7777-4709-8707-aa28fb86db9f", "dosage_form": "TABLET", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "50090-4608", "generic_name": "promethazine hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PROMETHAZINE HYDROCHLORIDE", "active_ingredients": [{"name": "PROMETHAZINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA040712", "marketing_category": "ANDA", "marketing_start_date": "20060731", "listing_expiration_date": "20261231"}