NDC 78206-152

PROPECIA

Finasteride

PROPECIA is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Organon Llc. The primary component is Finasteride.

• Product ID: 78206-152_2b0a9a40-71a2-4df2-9b97-d86095e40863
• NDC: 78206-152
• Product Type: Human Prescription Drug
• Proprietary Name: PROPECIA
• Generic Name: Finasteride
• Dosage Form: Tablet, Film Coated
• Route of Administration: ORAL
• Marketing Start Date: 2021-06-01
• Marketing Category: NDA /
• Application Number: NDA020788
• Labeler Name: Organon LLC
• Substance Name: FINASTERIDE
• Active Ingredient Strength: 1 mg/1
• Pharm Classes: 5-alpha Reductase Inhibitor [EPC],5-alpha Reductase Inhibitors [MoA]
• NDC Exclude Flag: N
• Listing Certified Through: 2022-12-31

Packaging

NDC 78206-152-01

30 TABLET, FILM COATED in 1 BOTTLE (78206-152-01)

• Marketing Start Date: 2021-06-01
• NDC Exclude Flag: N
• Sample Package?: N

Drug Details

NDC Crossover Matching brand name "PROPECIA" or generic name "Finasteride"

NDC	Brand Name	Generic Name
0006-0071	PROPECIA	finasteride
0093-7355	Finasteride	Finasteride
0179-0175	Finasteride	Finasteride
0378-5036	Finasteride	finasteride
0904-6830	Finasteride	Finasteride
16729-089	Finasteride	Finasteride
16729-090	Finasteride	finasteride
17856-0090	Finasteride	finasteride
31722-525	Finasteride	Finasteride
31722-526	Finasteride	Finasteride
33261-833	Finasteride	Finasteride
35573-400	Finasteride	Finasteride
42291-280	Finasteride	Finasteride
43598-303	Finasteride	Finasteride
43598-390	Finasteride	Finasteride
45963-500	Finasteride	Finasteride
45963-600	FINASTERIDE	FINASTERIDE
47335-714	Finasteride	Finasteride
47335-715	FINASTERIDE	FINASTERIDE
50090-1718	Finasteride	finasteride
0006-0072	PROSCAR	FINASTERIDE