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Triple Antibiotic HC

Neomycin and Polymyxin B Sulfates, Bacitracin Zinc and Hydrocortisone Ophthalmic Ointment, USP(Sterile)

Approved
Approval ID

8b45f06d-ad0b-447a-ab1d-14cab8ca4043

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Nov 4, 2010

Manufacturers
FDA

Phoenix Pharmaceutical, Inc.

DUNS: 150711039

Products 1

Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.

Neomycin sulfate and Polymyxin B Sulfate, Bacitracin Zinc and Hydrocortisone

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code57319-344
Application NumberANDA064068
Product Classification
M
Marketing Category
C73584
G
Generic Name
Neomycin sulfate and Polymyxin B Sulfate, Bacitracin Zinc and Hydrocortisone
Product Specifications
Route of AdministrationOPHTHALMIC
Effective DateOctober 5, 2010
FDA Product Classification

INGREDIENTS (6)

POLYMYXIN B SULFATEActive
Quantity: 10000 [USP'U] in 1 g
Code: 19371312D4
Classification: ACTIB
NEOMYCIN SULFATEActive
Quantity: 3.5 mg in 1 g
Code: 057Y626693
Classification: ACTIB
MINERAL OILInactive
Code: T5L8T28FGP
Classification: IACT
BACITRACIN ZINCActive
Quantity: 400 [USP'U] in 1 g
Code: 89Y4M234ES
Classification: ACTIB
HYDROCORTISONEActive
Quantity: 10 mg in 1 g
Code: WI4X0X7BPJ
Classification: ACTIB
PETROLATUMInactive
Code: 4T6H12BN9U
Classification: IACT

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Triple Antibiotic HC - FDA Drug Approval Details