NDC 41250-131

Ranitidine 75

Ranitidine Tablets

Ranitidine 75 is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by Meijer Distribution Inc. The primary component is Ranitidine Hydrochloride.

• Product ID: 41250-131_cabe7b1b-4c11-11f3-b279-21d271df7cd1
• NDC: 41250-131
• Product Type: Human Otc Drug
• Proprietary Name: Ranitidine 75
• Generic Name: Ranitidine Tablets
• Dosage Form: Tablet
• Route of Administration: ORAL
• Marketing Start Date: 2014-09-22
• Marketing Category: ANDA / ANDA
• Application Number: ANDA075294
• Labeler Name: Meijer Distribution Inc
• Substance Name: RANITIDINE HYDROCHLORIDE
• Active Ingredient Strength: 75 mg/1
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 41250-131-60

1 BOTTLE in 1 CARTON (41250-131-60) > 60 TABLET in 1 BOTTLE

• Marketing Start Date: 2014-09-22
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 41250-131-60 [41250013160]

Ranitidine 75 TABLET

• Marketing Category: ANDA
• Application Number: ANDA075294
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2014-09-22
• Marketing End Date: 2017-03-16

Drug Details

Active Ingredients

Ingredient	Strength
RANITIDINE HYDROCHLORIDE	75 mg/1

OpenFDA Data

• SPL SET ID: 1e3ca323-f936-e3dc-df25-65d2bcb2ce98
• Manufacturer:
  • Meijer Distribution Inc
• UNII:
  • BK76465IHM
• RxNorm Concept Unique ID - RxCUI:
  • 312773

NDC Crossover Matching brand name "Ranitidine 75" or generic name "Ranitidine Tablets"

NDC	Brand Name	Generic Name
0904-6715	ranitidine 75	Ranitidine
11673-131	Ranitidine 75	Ranitidine Tablets USP, 75mg
30142-131	Ranitidine 75	Ranitidine Tablets USP, 75mg
41250-131	Ranitidine 75	Ranitidine Tablets