NDC 68788-7388

Ranitidine

Ranitidine

Ranitidine is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Preferred Pharmaceuticals Inc.. The primary component is Ranitidine Hydrochloride.

• Product ID: 68788-7388_5598969e-12dd-4fec-9dbc-885c9971187f
• NDC: 68788-7388
• Product Type: Human Prescription Drug
• Proprietary Name: Ranitidine
• Generic Name: Ranitidine
• Dosage Form: Tablet, Film Coated
• Route of Administration: ORAL
• Marketing Start Date: 2016-09-16
• Marketing Category: ANDA / ANDA
• Application Number: ANDA078542
• Labeler Name: Preferred Pharmaceuticals Inc.
• Substance Name: RANITIDINE HYDROCHLORIDE
• Active Ingredient Strength: 150 mg/1
• Pharm Classes: Histamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 68788-7388-1

100 TABLET, FILM COATED in 1 BOTTLE (68788-7388-1)

• Marketing Start Date: 2016-09-16
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 68788-7388-1 [68788738801]

Ranitidine TABLET, FILM COATED

• Marketing Category: ANDA
• Application Number: ANDA078542
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2016-09-16

NDC 68788-7388-3 [68788738803]

Ranitidine TABLET, FILM COATED

• Marketing Category: ANDA
• Application Number: ANDA078542
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2016-09-16

NDC 68788-7388-6 [68788738806]

Ranitidine TABLET, FILM COATED

• Marketing Category: ANDA
• Application Number: ANDA078542
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2016-09-16

NDC 68788-7388-9 [68788738809]

Ranitidine TABLET, FILM COATED

• Marketing Category: ANDA
• Application Number: ANDA078542
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2016-09-16

NDC 68788-7388-8 [68788738808]

Ranitidine TABLET, FILM COATED

• Marketing Category: ANDA
• Application Number: ANDA078542
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2016-09-16

Drug Details

Active Ingredients

Ingredient	Strength
RANITIDINE HYDROCHLORIDE	150 mg/1

OpenFDA Data

• SPL SET ID: 390ca7d1-eb49-490d-82ed-34f656c7b2b2
• Manufacturer:
  • Preferred Pharmaceuticals Inc.
• UNII:
  • BK76465IHM
• RxNorm Concept Unique ID - RxCUI:
  • 198191

Pharmacological Class

• Histamine H2 Receptor Antagonists [MoA]
• Histamine-2 Receptor Antagonist [EPC]

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

NDC	Brand Name	Generic Name
0121-0727	Ranitidine	RANITIDINE
0121-4727	Ranitidine	RANITIDINE
0172-4357	Ranitidine	Ranitidine
0172-4358	Ranitidine	Ranitidine
0363-0352	Ranitidine	Ranitidine
0440-2300	Ranitidine	Ranitidine Hydrochloride
0440-8300	Ranitidine	Ranitidine
0440-8305	Ranitidine	Ranitidine
0615-4513	Ranitidine	Ranitidine
0615-4514	Ranitidine	Ranitidine
0615-8021	Ranitidine	Ranitidine
0781-6087	Ranitidine	Ranitidine
0904-6349	Ranitidine	Ranitidine
0904-6716	Ranitidine	Ranitidine
0904-6921	Ranitidine	Ranitidine
10544-056	Ranitidine	Ranitidine
10544-438	Ranitidine	Ranitidine
10544-516	Ranitidine	Ranitidine
68071-2190	Ranitidine	Ranitidine
68071-3162	Ranitidine	Ranitidine
68071-3317	Ranitidine	Ranitidine
68071-2185	Ranitidine	Ranitidine
68071-3248	Ranitidine	Ranitidine
68071-3165	Ranitidine	Ranitidine
68151-1610	Ranitidine	Ranitidine
68151-2890	Ranitidine	Ranitidine
68462-248	Ranitidine	Ranitidine
68462-249	Ranitidine	Ranitidine
68788-6382	Ranitidine	Ranitidine
68788-7101	Ranitidine	Ranitidine
68788-7078	Ranitidine	Ranitidine
68788-7388	Ranitidine	Ranitidine
68788-9875	Ranitidine	Ranitidine
68788-9874	Ranitidine	Ranitidine
70408-141	RANITIDINE	RANITIDINE
70518-0222	Ranitidine	Ranitidine
70518-0263	Ranitidine	Ranitidine
70518-0093	Ranitidine	Ranitidine
70518-0622	Ranitidine	Ranitidine
70518-0873	Ranitidine	Ranitidine
70518-0801	Ranitidine	Ranitidine
70518-1361	Ranitidine	Ranitidine
70518-1714	Ranitidine	Ranitidine
70934-017	Ranitidine	Ranitidine
71141-013	Ranitidine	Ranitidine
71335-0394	Ranitidine	Ranitidine
71335-0342	Ranitidine	Ranitidine
71335-0363	Ranitidine	Ranitidine
71821-001	Ranitidine	Ranitidine
71821-002	Ranitidine	Ranitidine