NDC 0299-5935

AKLIEF

Trifarotene

AKLIEF is a Topical Cream in the Human Prescription Drug category. It is labeled and distributed by Galderma Laboratories, L.p.. The primary component is Trifarotene.

• Product ID: 0299-5935_19ffc4da-a632-4497-830c-504edf4536c8
• NDC: 0299-5935
• Product Type: Human Prescription Drug
• Proprietary Name: AKLIEF
• Generic Name: Trifarotene
• Dosage Form: Cream
• Route of Administration: TOPICAL
• Marketing Start Date: 2019-10-04
• Marketing Category: NDA / NDA
• Application Number: NDA211527
• Labeler Name: Galderma Laboratories, L.P.
• Substance Name: TRIFAROTENE
• Active Ingredient Strength: 50 ug/g
• NDC Exclude Flag: N
• Listing Certified Through: 2021-12-31

Packaging

NDC 0299-5935-02

1 TUBE in 1 BLISTER PACK (0299-5935-02) > 2 g in 1 TUBE

• Marketing Start Date: 2019-10-04
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 0299-5935-30 [00299593530]

AKLIEF CREAM

• Marketing Category: NDA
• Application Number: NDA211527
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2019-10-04

NDC 0299-5935-02 [00299593502]

AKLIEF CREAM

• Marketing Category: NDA
• Application Number: NDA211527
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2019-10-04

NDC 0299-5935-75 [00299593575]

AKLIEF CREAM

• Marketing Category: NDA
• Application Number: NDA211527
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2019-10-04

NDC 0299-5935-45 [00299593545]

AKLIEF CREAM

• Marketing Category: NDA
• Application Number: NDA211527
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: GM
• Marketing Start Date: 2019-10-04

Drug Details

Active Ingredients

Ingredient	Strength
TRIFAROTENE	50 ug/g