neomycin and polymyxin b sulfates and hydrocortisone

Generic: neomycin sulfate, polymyxin b sulfate and hydrocortisone

Labeler: preferred pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name neomycin and polymyxin b sulfates and hydrocortisone
Generic Name neomycin sulfate, polymyxin b sulfate and hydrocortisone
Labeler preferred pharmaceuticals, inc.
Dosage Form SUSPENSION/ DROPS
Routes
AURICULAR (OTIC)
Active Ingredients

hydrocortisone 10 mg/mL, neomycin sulfate 3.5 mg/mL, polymyxin b sulfate 10000 [USP'U]/mL

Manufacturer
Preferred Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 68788-9924
Product ID 68788-9924_cee1c117-8586-4735-aab3-8eeb4ed195ba
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA064065
Listing Expiration 2026-12-31
Marketing Start 2012-01-18

Pharmacologic Class

Established (EPC)
corticosteroid [epc]
Mechanism of Action
corticosteroid hormone receptor agonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 687889924
Hyphenated Format 68788-9924

Supplemental Identifiers

RxCUI
310687
UNII
WI4X0X7BPJ 057Y626693 19371312D4
NUI
N0000175576 N0000175450

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 neomycin and polymyxin b sulfates and hydrocortisone (source: ndc)
Generic Name neomycin sulfate, polymyxin b sulfate and hydrocortisone (source: ndc)
Application Number ANDA064065 (source: ndc)
Routes
AURICULAR (OTIC)
source: ndc

Resolved Composition

Strengths
  • 10 mg/mL
  • 3.5 mg/mL
  • 10000 [USP'U]/mL
source: ndc
Packaging
  • 1 BOTTLE, DROPPER in 1 CARTON (68788-9924-1) / 10 mL in 1 BOTTLE, DROPPER
source: ndc

Packages (1)

Ingredients (3)

hydrocortisone (10 mg/mL) neomycin sulfate (3.5 mg/mL) polymyxin b sulfate (10000 [USP'U]/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["AURICULAR (OTIC)"], "spl_id": "cee1c117-8586-4735-aab3-8eeb4ed195ba", "openfda": {"nui": ["N0000175576", "N0000175450"], "unii": ["WI4X0X7BPJ", "057Y626693", "19371312D4"], "rxcui": ["310687"], "spl_set_id": ["f8dc2b6f-daf3-4a3a-b31f-b97e2f152eae"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["Preferred Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, DROPPER in 1 CARTON (68788-9924-1)  / 10 mL in 1 BOTTLE, DROPPER", "package_ndc": "68788-9924-1", "marketing_start_date": "20120118"}], "brand_name": "Neomycin and Polymyxin B Sulfates and Hydrocortisone", "product_id": "68788-9924_cee1c117-8586-4735-aab3-8eeb4ed195ba", "dosage_form": "SUSPENSION/ DROPS", "pharm_class": ["Aminoglycoside Antibacterial [EPC]", "Aminoglycosides [CS]", "Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]", "Polymyxin-class Antibacterial [EPC]", "Polymyxins [CS]"], "product_ndc": "68788-9924", "generic_name": "Neomycin sulfate, Polymyxin B Sulfate and Hydrocortisone", "labeler_name": "Preferred Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Neomycin and Polymyxin B Sulfates and Hydrocortisone", "active_ingredients": [{"name": "HYDROCORTISONE", "strength": "10 mg/mL"}, {"name": "NEOMYCIN SULFATE", "strength": "3.5 mg/mL"}, {"name": "POLYMYXIN B SULFATE", "strength": "10000 [USP'U]/mL"}], "application_number": "ANDA064065", "marketing_category": "ANDA", "marketing_start_date": "20120118", "listing_expiration_date": "20261231"}