NDC 70771-1152

Finasteride

Finasteride

Finasteride is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Zydus Lifesciences Limited. The primary component is Finasteride.

• Product ID: 70771-1152_5068fb9d-4d3e-4ebc-ac25-5a42a89a5efc
• NDC: 70771-1152
• Product Type: Human Prescription Drug
• Proprietary Name: Finasteride
• Generic Name: Finasteride
• Dosage Form: Tablet, Film Coated
• Route of Administration: ORAL
• Marketing Start Date: 2017-12-05
• Marketing Category: ANDA / ANDA
• Application Number: ANDA078900
• Labeler Name: Zydus Lifesciences Limited
• Substance Name: FINASTERIDE
• Active Ingredient Strength: 5 mg/1
• Pharm Classes: 5-alpha Reductase Inhibitor [EPC], 5-alpha Reductase Inhibitors [MoA]
• NDC Exclude Flag: N
• Listing Certified Through: 2023-12-31

Packaging

NDC 70771-1152-0

1000 TABLET, FILM COATED in 1 BOTTLE (70771-1152-0)

• Marketing Start Date: 2017-12-05
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 70771-1152-0 [70771115200]

Finasteride TABLET, FILM COATED

• Marketing Category: ANDA
• Application Number: ANDA078900
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2017-12-05

NDC 70771-1152-1 [70771115201]

Finasteride TABLET, FILM COATED

• Marketing Category: ANDA
• Application Number: ANDA078900
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2017-12-05

NDC 70771-1152-4 [70771115204]

Finasteride TABLET, FILM COATED

• Marketing Category: ANDA
• Application Number: ANDA078900
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2017-12-05

NDC 70771-1152-3 [70771115203]

Finasteride TABLET, FILM COATED

• Marketing Category: ANDA
• Application Number: ANDA078900
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2017-12-05

Drug Details

Active Ingredients

Ingredient	Strength
FINASTERIDE	5 mg/1

OpenFDA Data

• SPL SET ID: 16c0be08-b6af-4cb1-b20f-9934c9f78d32
• Manufacturer:
  • Cadila Healthcare Limited
• UNII:
  • 57GNO57U7G
• RxNorm Concept Unique ID - RxCUI:
  • 310346

Pharmacological Class

• 5-alpha Reductase Inhibitor [EPC]
• 5-alpha Reductase Inhibitors [MoA]

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

NDC	Brand Name	Generic Name
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
67877-288	Finasteride	Finasteride
67877-455	Finasteride	Finasteride
68071-1648	Finasteride	Finasteride
68071-1710	Finasteride	Finasteride
68071-3234	Finasteride	Finasteride
68071-3306	Finasteride	Finasteride
68071-4044	Finasteride	Finasteride
68071-3354	Finasteride	Finasteride
68071-3380	Finasteride	Finasteride
68071-4167	Finasteride	Finasteride
68071-4541	Finasteride	Finasteride
68071-4808	Finasteride	Finasteride
68084-399	Finasteride	Finasteride
68382-074	Finasteride	Finasteride
68645-541	Finasteride	Finasteride
68554-3026	Finasteride	Finasteride
68554-3025	Finasteride	Finasteride
68788-6976	Finasteride	Finasteride
68788-6875	Finasteride	Finasteride
68788-9519	Finasteride	Finasteride
68788-9249	Finasteride	Finasteride
68788-9517	Finasteride	Finasteride
69097-112	Finasteride	Finasteride
70518-0397	Finasteride	Finasteride
70518-1704	Finasteride	Finasteride
70771-1152	Finasteride	Finasteride
71335-0433	Finasteride	Finasteride
71335-0281	Finasteride	Finasteride
71335-0235	Finasteride	Finasteride
76282-412	Finasteride	Finasteride
76519-1204	FINASTERIDE	FINASTERIDE