promethazine hydrochloride
Generic: promethazine hydrochloride
Labeler: xttrium laboratories, inc.Drug Facts
Product Profile
Brand Name
promethazine hydrochloride
Generic Name
promethazine hydrochloride
Labeler
xttrium laboratories, inc.
Dosage Form
SYRUP
Routes
Active Ingredients
promethazine hydrochloride 6.25 mg/5mL
Manufacturer
Identifiers & Regulatory
Product NDC
0116-4023
Product ID
0116-4023_302bfe23-7984-140e-e063-6394a90acad1
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA087953
Listing Expiration
2026-12-31
Marketing Start
2025-04-07
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
01164023
Hyphenated Format
0116-4023
Supplemental Identifiers
RxCUI
UPC
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
ANDA087953 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 6.25 mg/5mL
Packaging
- 473 mL in 1 BOTTLE, PLASTIC (0116-4023-16)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "302bfe23-7984-140e-e063-6394a90acad1", "openfda": {"upc": ["0301164023165"], "unii": ["R61ZEH7I1I"], "rxcui": ["992432"], "spl_set_id": ["302bfea2-d403-d315-e063-6294a90a37dd"], "manufacturer_name": ["Xttrium Laboratories, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE, PLASTIC (0116-4023-16)", "package_ndc": "0116-4023-16", "marketing_start_date": "20250407"}], "brand_name": "PROMETHAZINE HYDROCHLORIDE", "product_id": "0116-4023_302bfe23-7984-140e-e063-6394a90acad1", "dosage_form": "SYRUP", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "0116-4023", "generic_name": "promethazine hydrochloride", "labeler_name": "Xttrium Laboratories, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PROMETHAZINE HYDROCHLORIDE", "active_ingredients": [{"name": "PROMETHAZINE HYDROCHLORIDE", "strength": "6.25 mg/5mL"}], "application_number": "ANDA087953", "marketing_category": "ANDA", "marketing_start_date": "20250407", "listing_expiration_date": "20261231"}