NDC 72356-101

AMZEEQ

Minocycline

AMZEEQ is a Topical Aerosol, Foam in the Human Prescription Drug category. It is labeled and distributed by Journey Medical Corporation. The primary component is Minocycline Hydrochloride.

• Product ID: 72356-101_0aebe7ba-e714-4400-9197-239b9db39788
• NDC: 72356-101
• Product Type: Human Prescription Drug
• Proprietary Name: AMZEEQ
• Generic Name: Minocycline
• Dosage Form: Aerosol, Foam
• Route of Administration: TOPICAL
• Marketing Start Date: 2020-01-02
• Marketing Category: NDA / NDA
• Application Number: NDA212379
• Labeler Name: Journey Medical Corporation
• Substance Name: MINOCYCLINE HYDROCHLORIDE
• Active Ingredient Strength: 40 mg/g
• Pharm Classes: Tetracycline-class Drug [EPC], Tetracyclines [CS]
• NDC Exclude Flag: N
• Listing Certified Through: 2023-12-31

Packaging

NDC 72356-101-03

1 CAN in 1 CARTON (72356-101-03) > 30 g in 1 CAN

• Marketing Start Date: 2020-01-02
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 72356-101-90 [72356010190]

AMZEEQ AEROSOL, FOAM

• Marketing Category: NDA
• Application Number: NDA212379
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2020-01-02

NDC 72356-101-03 [72356010103]

AMZEEQ AEROSOL, FOAM

• Marketing Category: NDA
• Application Number: NDA212379
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: GM
• Marketing Start Date: 2020-01-02

Drug Details

Active Ingredients

Ingredient	Strength
MINOCYCLINE HYDROCHLORIDE	40 mg/g

NDC Crossover Matching brand name "AMZEEQ" or generic name "Minocycline"

NDC	Brand Name	Generic Name
69489-201	AMZEEQ	Minocycline
72356-101	AMZEEQ	Minocycline
42291-589	Minocycline	Minocycline
42291-591	Minocycline	Minocycline
49884-511	Minocycline	Minocycline
49884-512	Minocycline	Minocycline
49884-513	Minocycline	Minocycline
63629-2228	Minocycline	Minocycline
63629-2229	Minocycline	Minocycline
69489-212	ZILXI	Minocycline
72356-103	ZILXI	Minocycline