ranitidine hydrochloride

Generic: ranitidine hydrochloride

Labeler: dr. reddy's laboratories limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ranitidine hydrochloride
Generic Name ranitidine hydrochloride
Labeler dr. reddy's laboratories limited
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

ranitidine hydrochloride 300 mg/1

Manufacturer
Dr. Reddy's Laboratories Limited

Identifiers & Regulatory

Product NDC 55111-130
Product ID 55111-130_9741e6f4-a2dc-7543-1138-da97eafe11bd
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075742
Listing Expiration 2026-12-31
Marketing Start 2001-04-01

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 55111130
Hyphenated Format 55111-130

Supplemental Identifiers

RxCUI
198190 198192
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 hydrochloride (source: ndc)
Generic Name ranitidine hydrochloride (source: ndc)
Application Number ANDA075742 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 300 mg/1
source: ndc
Packaging
  • 100 CAPSULE in 1 BOTTLE (55111-130-01)
  • 30 CAPSULE in 1 BOTTLE (55111-130-30)
source: ndc

Packages (2)

55111-130-01 100 CAPSULE in 1 BOTTLE (55111-130-01) 55111-130-30 30 CAPSULE in 1 BOTTLE (55111-130-30)

Ingredients (1)

ranitidine hydrochloride (300 mg/1)

Linked Drug Pages (1)

Ranitidine Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "9741e6f4-a2dc-7543-1138-da97eafe11bd", "openfda": {"unii": ["BK76465IHM"], "rxcui": ["198190", "198192"], "spl_set_id": ["7bf94bf7-fa11-70be-9f65-fe26a3db5a63"], "manufacturer_name": ["Dr. Reddy's Laboratories Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (55111-130-01)", "package_ndc": "55111-130-01", "marketing_start_date": "20010401"}, {"sample": false, "description": "30 CAPSULE in 1 BOTTLE (55111-130-30)", "package_ndc": "55111-130-30", "marketing_start_date": "20010401"}], "brand_name": "Ranitidine Hydrochloride", "product_id": "55111-130_9741e6f4-a2dc-7543-1138-da97eafe11bd", "dosage_form": "CAPSULE", "pharm_class": ["Histamine H2 Receptor Antagonists [MoA]", "Histamine-2 Receptor Antagonist [EPC]"], "product_ndc": "55111-130", "generic_name": "Ranitidine Hydrochloride", "labeler_name": "Dr. Reddy's Laboratories Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ranitidine Hydrochloride", "active_ingredients": [{"name": "RANITIDINE HYDROCHLORIDE", "strength": "300 mg/1"}], "application_number": "ANDA075742", "marketing_category": "ANDA", "marketing_start_date": "20010401", "listing_expiration_date": "20261231"}