ranitidine

Generic: ranitidine

Labeler: ajanta pharma usa inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ranitidine
Generic Name ranitidine
Labeler ajanta pharma usa inc.
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

ranitidine hydrochloride 150 mg/1

Manufacturer
Ajanta Pharma USA Inc.

Identifiers & Regulatory

Product NDC 27241-109
Product ID 27241-109_d7fd99da-f17a-4124-9014-70bbe43d78f6
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA209859
Listing Expiration 2026-12-31
Marketing Start 2018-09-27

Pharmacologic Class

Classes
histamine h2 receptor antagonists [moa] histamine-2 receptor antagonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 27241109
Hyphenated Format 27241-109

Supplemental Identifiers

RxCUI
198190 198192
UPC
0327241110030 0327241109065
UNII
BK76465IHM

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name ranitidine (source: ndc)
Generic Name ranitidine (source: ndc)
Application Number ANDA209859 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 150 mg/1
source: ndc
Packaging
  • 60 CAPSULE in 1 BOTTLE (27241-109-06)
  • 500 CAPSULE in 1 BOTTLE (27241-109-50)
source: ndc

Packages (2)

27241-109-06 60 CAPSULE in 1 BOTTLE (27241-109-06) 27241-109-50 500 CAPSULE in 1 BOTTLE (27241-109-50)

Ingredients (1)

ranitidine hydrochloride (150 mg/1)

Linked Drug Pages (1)

Ranitidine ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "d7fd99da-f17a-4124-9014-70bbe43d78f6", "openfda": {"upc": ["0327241110030", "0327241109065"], "unii": ["BK76465IHM"], "rxcui": ["198190", "198192"], "spl_set_id": ["fb67e8c7-b817-4253-a1a1-5ecdcee694cf"], "manufacturer_name": ["Ajanta Pharma USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 CAPSULE in 1 BOTTLE (27241-109-06)", "package_ndc": "27241-109-06", "marketing_start_date": "20180927"}, {"sample": false, "description": "500 CAPSULE in 1 BOTTLE (27241-109-50)", "package_ndc": "27241-109-50", "marketing_start_date": "20180927"}], "brand_name": "Ranitidine", "product_id": "27241-109_d7fd99da-f17a-4124-9014-70bbe43d78f6", "dosage_form": "CAPSULE", "pharm_class": ["Histamine H2 Receptor Antagonists [MoA]", "Histamine-2 Receptor Antagonist [EPC]"], "product_ndc": "27241-109", "generic_name": "Ranitidine", "labeler_name": "Ajanta Pharma USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ranitidine", "active_ingredients": [{"name": "RANITIDINE HYDROCHLORIDE", "strength": "150 mg/1"}], "application_number": "ANDA209859", "marketing_category": "ANDA", "marketing_start_date": "20180927", "listing_expiration_date": "20261231"}