NDC 68998-397

Ranitidine 150

Ranitidine Hcl Tablets 150mg

Ranitidine 150 is a Oral Tablet, Coated in the Human Otc Drug category. It is labeled and distributed by Marc Glassman, Inc.. The primary component is Ranitidine Hydrochloride.

• Product ID: 68998-397_0d136b75-d474-492c-bc8f-737fa3d31592
• NDC: 68998-397
• Product Type: Human Otc Drug
• Proprietary Name: Ranitidine 150
• Generic Name: Ranitidine Hcl Tablets 150mg
• Dosage Form: Tablet, Coated
• Route of Administration: ORAL
• Marketing Start Date: 2018-10-01
• Marketing Category: ANDA / ANDA
• Application Number: ANDA078192
• Labeler Name: Marc Glassman, Inc.
• Substance Name: RANITIDINE HYDROCHLORIDE
• Active Ingredient Strength: 150 mg/1
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 68998-397-93

2 BLISTER PACK in 1 CARTON (68998-397-93) > 12 TABLET, COATED in 1 BLISTER PACK

• Marketing Start Date: 2018-10-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 68998-397-93 [68998039793]

Ranitidine 150 TABLET, COATED

• Marketing Category: ANDA
• Application Number: ANDA078192
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2018-10-01

Drug Details

Active Ingredients

Ingredient	Strength
RANITIDINE HYDROCHLORIDE	150 mg/1

OpenFDA Data

• SPL SET ID: ae10fb7a-cfa4-4707-acc4-67856c41e9b3
• Manufacturer:
  • Marc Glassman, Inc.
• UNII:
  • BK76465IHM
• RxNorm Concept Unique ID - RxCUI:
  • 198191

NDC Crossover Matching brand name "Ranitidine 150" or generic name "Ranitidine Hcl Tablets 150mg"

NDC	Brand Name	Generic Name
49035-404	Ranitidine 150	Ranitidine Hydrochloride Tablets 150mg
68998-375	Ranitidine 150	Ranitidine HCl Tablets 150mg
68998-397	Ranitidine 150	Ranitidine HCl Tablets 150mg
69168-375	Ranitidine 150	Ranitidine Hydrochloride Tablets 150mg
69168-389	Ranitidine 150	Ranitidine Hydrochloride Tablets 150mg
69168-397	Ranitidine 150	Ranitidine HCl Tablets 150mg
69168-902	Ranitidine 150	Ranitidine HCl Tablets 150mg