NDC 70934-017

Ranitidine

Ranitidine

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

• Product ID: 70934-017_795e44d4-df4d-011d-e053-2991aa0a129f
• NDC: 70934-017
• Product Type: Human Prescription Drug
• Proprietary Name: Ranitidine
• Generic Name: Ranitidine
• Dosage Form: Tablet, Film Coated
• Route of Administration: ORAL
• Marketing Start Date: 2018-10-25
• Marketing Category: ANDA / ANDA
• Application Number: ANDA078542
• Labeler Name: Denton Pharma, Inc. DBA Northwind Pharmaceuticals
• 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: 2019-12-31

Packaging

NDC 70934-017-20

20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-017-20)

• Marketing Start Date: 2018-10-25
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 70934-017-04 [70934001704]

Ranitidine TABLET, FILM COATED

• Marketing Category: ANDA
• Application Number: ANDA078542
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2019-06-03
• Marketing End Date: 2020-04-30

NDC 70934-017-24 [70934001724]

Ranitidine TABLET, FILM COATED

• Marketing Category: ANDA
• Application Number: ANDA078542
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2019-04-17
• Marketing End Date: 2020-04-30

NDC 70934-017-30 [70934001730]

Ranitidine TABLET, FILM COATED

• Marketing Category: ANDA
• Application Number: ANDA078542
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2019-07-17
• Marketing End Date: 2020-04-30

NDC 70934-017-20 [70934001720]

Ranitidine TABLET, FILM COATED

• Marketing Category: ANDA
• Application Number: ANDA078542
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2018-10-25
• Marketing End Date: 2020-04-30

NDC 70934-017-90 [70934001790]

Ranitidine TABLET, FILM COATED

• Marketing Category: ANDA
• Application Number: ANDA078542
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2019-04-25
• Marketing End Date: 2020-04-30

Drug Details

Active Ingredients

Ingredient	Strength
RANITIDINE HYDROCHLORIDE	150 mg/1

OpenFDA Data

• SPL SET ID: 795e44d4-df4c-011d-e053-2991aa0a129f
• Manufacturer:
  • Denton Pharma, Inc. DBA Northwind Pharmaceuticals
• 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