NDC 0378-8085

Tretionin

Tretionin

Tretionin is a Topical Gel in the Human Prescription Drug category. It is labeled and distributed by Mylan Pharmaceuticals Inc.. The primary component is Tretinoin.

• Product ID: 0378-8085_22767e97-7665-4f39-9cbf-af0025526a15
• NDC: 0378-8085
• Product Type: Human Prescription Drug
• Proprietary Name: Tretionin
• Generic Name: Tretionin
• Dosage Form: Gel
• Route of Administration: TOPICAL
• Marketing Start Date: 2018-11-05
• Marketing Category: NDA AUTHORIZED GENERIC / NDA AUTHORIZED GENERIC
• Application Number: NDA017955
• Labeler Name: Mylan Pharmaceuticals Inc.
• Substance Name: TRETINOIN
• Active Ingredient Strength: 0 mg/g
• Pharm Classes: Retinoid [EPC],Retinoids [CS]
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 0378-8085-15

1 TUBE in 1 CARTON (0378-8085-15) > 15 g in 1 TUBE

• Marketing Start Date: 2019-08-12
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 0378-8085-15 [00378808515]

Tretionin GEL

• Marketing Category: NDA authorized generic
• Application Number: NDA017955
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: GM
• Marketing Start Date: 2019-08-12

NDC 0378-8085-45 [00378808545]

Tretionin GEL

• Marketing Category: NDA authorized generic
• Application Number: NDA017955
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: GM
• Marketing Start Date: 2019-08-12

Drug Details

Pharmacological Class

• Retinoid [EPC]
• Retinoids [CS]

NDC Crossover Matching brand name "Tretionin" or generic name "Tretionin"

NDC	Brand Name	Generic Name
0378-8082	Tretionin	Tretionin
0378-8083	Tretionin	Tretionin
0378-8084	Tretionin	Tretionin
0378-8085	Tretionin	Tretionin
0378-8086	Tretionin	Tretionin