NDC 23594-780

Ulesfia

Benzyl Alcohol

Ulesfia is a Topical Lotion in the Human Prescription Drug category. It is labeled and distributed by Cerecor, Inc.. The primary component is Benzyl Alcohol.

• Product ID: 23594-780_3f0364fa-e779-4522-84ca-a5229ee3ca52
• NDC: 23594-780
• Product Type: Human Prescription Drug
• Proprietary Name: Ulesfia
• Generic Name: Benzyl Alcohol
• Dosage Form: Lotion
• Route of Administration: TOPICAL
• Marketing Start Date: 2014-07-16
• Marketing Category: NDA / NDA
• Application Number: NDA022129
• Labeler Name: Cerecor, Inc.
• Substance Name: BENZYL ALCOHOL
• Active Ingredient Strength: 50 mg/g
• Pharm Classes: Pediculicide [EPC]
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 23594-780-88

2 BOTTLE, PLASTIC in 1 CARTON (23594-780-88) > 227 g in 1 BOTTLE, PLASTIC

• Marketing Start Date: 2014-07-16
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 23594-780-08 [23594078008]

Ulesfia LOTION

• Marketing Category: NDA
• Application Number: NDA022129
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2014-07-16

NDC 23594-780-88 [23594078088]

Ulesfia LOTION

• Marketing Category: NDA
• Application Number: NDA022129
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: GM
• Marketing Start Date: 2014-07-16

Drug Details

Active Ingredients

Ingredient	Strength
BENZYL ALCOHOL	50 mg/g

Pharmacological Class

• Pediculicide [EPC]

Medicade Reported Pricing

23594078088 ULESFIA 5% LOTION

Pricing Unit: GM | Drug Type:

NDC Crossover Matching brand name "Ulesfia" or generic name "Benzyl Alcohol"

NDC	Brand Name	Generic Name
23594-780	Ulesfia	benzyl alcohol
69202-780	Ulesfia	benzyl alcohol
54866-002	AVERTEAX	Benzyl Alcohol
71416-001	Protocoxil	BENZYL ALCOHOL
50486-468	Zilactin	benzyl alcohol
72751-0301	Zilactin	benzyl alcohol