promethazine hydrochloride

Generic: promethazine hydrochloride

Labeler: xttrium laboratories, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name promethazine hydrochloride
Generic Name promethazine hydrochloride
Labeler xttrium laboratories, inc.
Dosage Form SYRUP
Routes
ORAL
Active Ingredients

promethazine hydrochloride 6.25 mg/5mL

Manufacturer
Xttrium Laboratories, Inc.

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
phenothiazine [epc] phenothiazines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 01164023
Hyphenated Format 0116-4023

Supplemental Identifiers

RxCUI
992432
UPC
0301164023165
UNII
R61ZEH7I1I

Packaging Origin

Original Packager
true

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
ORAL
source: ndc

Resolved Composition

Strengths
  • 6.25 mg/5mL
source: ndc
Packaging
  • 473 mL in 1 BOTTLE, PLASTIC (0116-4023-16)
source: ndc

Packages (1)

Ingredients (1)

promethazine hydrochloride (6.25 mg/5mL)

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"}