NDC 66715-9758

Zantac 360

Famotidine Tablet, Film-coated

Zantac 360 is a Oral Tablet, Film Coated in the Human Otc Drug category. It is labeled and distributed by Lil' Drug Store Products, Inc. The primary component is Famotidine.

• Product ID: 66715-9758_ea38535a-c9dc-d03f-e053-2a95a90adf2d
• NDC: 66715-9758
• Product Type: Human Otc Drug
• Proprietary Name: Zantac 360
• Generic Name: Famotidine Tablet, Film-coated
• Dosage Form: Tablet, Film Coated
• Route of Administration: ORAL
• Marketing Start Date: 2021-09-20
• Marketing Category: ANDA /
• Application Number: ANDA206531
• Labeler Name: Lil' Drug Store Products, Inc
• Substance Name: FAMOTIDINE
• Active Ingredient Strength: 20 mg/1
• Pharm Classes: Histamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]
• NDC Exclude Flag: N
• Listing Certified Through: 2023-12-31

Packaging

NDC 66715-9758-5

1 BLISTER PACK in 1 CARTON (66715-9758-5) > 5 TABLET, FILM COATED in 1 BLISTER PACK

• Marketing Start Date: 2021-09-20
• NDC Exclude Flag: N
• Sample Package?: N

Drug Details

NDC Crossover Matching brand name "Zantac 360" or generic name "Famotidine Tablet, Film-coated"

NDC	Brand Name	Generic Name
41167-0360	Zantac 360	Famotidine
41167-0361	Zantac 360	Famotidine
52904-926	Zantac 360	famotidine
66715-9758	Zantac 360	Famotidine tablet, film-coated
67751-214	Zantac 360	Famotidine