ranitidine

Generic: ranitidine

Labeler: granules india ltd
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ranitidine
Generic Name ranitidine
Labeler granules india ltd
Dosage Form TABLET
Routes
ORAL
Active Ingredients

ranitidine hydrochloride 150 mg/1

Manufacturer
Granules India Ltd

Identifiers & Regulatory

Product NDC 62207-773
Product ID 62207-773_44f2b222-ae43-eef4-e063-6394a90ab2b6
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA210243
Listing Expiration 2026-12-31
Marketing Start 2019-06-26

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 62207773
Hyphenated Format 62207-773

Supplemental Identifiers

RxCUI
198191
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 ANDA210243 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 150 mg/1
source: ndc
Packaging
  • 5 BAG in 1 CARTON (62207-773-36) / 10000 TABLET in 1 BAG (62207-773-32)
  • 1 BOTTLE in 1 CARTON (62207-773-41) / 24 TABLET in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (62207-773-47) / 500 TABLET in 1 BOTTLE
  • 2 BLISTER PACK in 1 CARTON (62207-773-58) / 10 TABLET in 1 BLISTER PACK
source: ndc

Packages (4)

62207-773-36 5 BAG in 1 CARTON (62207-773-36) / 10000 TABLET in 1 BAG (62207-773-32) 62207-773-41 1 BOTTLE in 1 CARTON (62207-773-41) / 24 TABLET in 1 BOTTLE 62207-773-47 1 BOTTLE in 1 CARTON (62207-773-47) / 500 TABLET in 1 BOTTLE 62207-773-58 2 BLISTER PACK in 1 CARTON (62207-773-58) / 10 TABLET in 1 BLISTER PACK

Ingredients (1)

ranitidine hydrochloride (150 mg/1)

Linked Drug Pages (1)

Ranitidine, Ranitidine cool mint ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "44f2b222-ae43-eef4-e063-6394a90ab2b6", "openfda": {"unii": ["BK76465IHM"], "rxcui": ["198191"], "spl_set_id": ["aab81d9f-397d-49fb-8083-77a1872cc71f"], "manufacturer_name": ["Granules India Ltd"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "5 BAG in 1 CARTON (62207-773-36)  / 10000 TABLET in 1 BAG (62207-773-32)", "package_ndc": "62207-773-36", "marketing_start_date": "20190626"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (62207-773-41)  / 24 TABLET in 1 BOTTLE", "package_ndc": "62207-773-41", "marketing_start_date": "20190626"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (62207-773-47)  / 500 TABLET in 1 BOTTLE", "package_ndc": "62207-773-47", "marketing_start_date": "20190626"}, {"sample": false, "description": "2 BLISTER PACK in 1 CARTON (62207-773-58)  / 10 TABLET in 1 BLISTER PACK", "package_ndc": "62207-773-58", "marketing_start_date": "20190626"}], "brand_name": "Ranitidine", "product_id": "62207-773_44f2b222-ae43-eef4-e063-6394a90ab2b6", "dosage_form": "TABLET", "pharm_class": ["Histamine H2 Receptor Antagonists [MoA]", "Histamine-2 Receptor Antagonist [EPC]"], "product_ndc": "62207-773", "generic_name": "Ranitidine", "labeler_name": "Granules India Ltd", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Ranitidine", "active_ingredients": [{"name": "RANITIDINE HYDROCHLORIDE", "strength": "150 mg/1"}], "application_number": "ANDA210243", "marketing_category": "ANDA", "marketing_start_date": "20190626", "listing_expiration_date": "20261231"}