NDC 67751-214

Zantac 360

Famotidine

Zantac 360 is a Oral Tablet, Film Coated in the Human Otc Drug category. It is labeled and distributed by Navajo Manufacturing Company Inc.. The primary component is Famotidine.

• Product ID: 67751-214_e3278e75-9ba1-546e-e053-2995a90af170
• NDC: 67751-214
• Product Type: Human Otc Drug
• Proprietary Name: Zantac 360
• Generic Name: Famotidine
• Dosage Form: Tablet, Film Coated
• Route of Administration: ORAL
• Marketing Start Date: 2022-08-01
• Marketing Category: ANDA /
• Application Number: ANDA206531
• Labeler Name: Navajo Manufacturing Company 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 67751-214-01

1 BLISTER PACK in 1 CARTON (67751-214-01) > 1 TABLET, FILM COATED in 1 BLISTER PACK

• Marketing Start Date: 2022-08-01
• NDC Exclude Flag: N
• Sample Package?: N

Drug Details

NDC Crossover Matching brand name "Zantac 360" or generic name "Famotidine"

NDC	Brand Name	Generic Name
0363-0141	Acid Controller	Famotidine
0363-0701	Acid Controller	Famotidine
0363-1203	acid controller	famotidine
0113-7141	basic care acid reducer	Famotidine
0113-7194	Basic Care famotidine	Famotidine
0093-2748	Famotidine	Famotidine
0172-5728	Famotidine	Famotidine
0172-5729	Famotidine	Famotidine
0338-5197	Famotidine	Famotidine
0363-0036	Famotidine	Famotidine
0363-1899	Famotidine	Famotidine
0113-0141	good sense acid reducer	Famotidine
0113-0194	Good Sense Acid Reducer	Famotidine
0187-4420	Pepcid	famotidine
0187-4440	Pepcid	famotidine