cimetidine

Generic: cimetidine

Labeler: northwind health company, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name cimetidine
Generic Name cimetidine
Labeler northwind health company, llc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

cimetidine 400 mg/1

Manufacturer
Northwind Health Company, LLC

Identifiers & Regulatory

Product NDC 51655-697
Product ID 51655-697_4950cd76-c47b-d0cf-e063-6394a90acf6d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA074246
Listing Expiration 2027-12-31
Marketing Start 2021-04-01

Pharmacologic Class

Established (EPC)
histamine-2 receptor antagonist [epc]
Mechanism of Action
histamine h2 receptor antagonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 51655697
Hyphenated Format 51655-697

Supplemental Identifiers

RxCUI
197507
UNII
80061L1WGD
NUI
N0000000151 N0000175784

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 cimetidine (source: ndc)
Generic Name cimetidine (source: ndc)
Application Number ANDA074246 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 400 mg/1
source: ndc
Packaging
  • 40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-697-51)
source: ndc

Packages (1)

Ingredients (1)

cimetidine (400 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4950cd76-c47b-d0cf-e063-6394a90acf6d", "openfda": {"nui": ["N0000000151", "N0000175784"], "unii": ["80061L1WGD"], "rxcui": ["197507"], "spl_set_id": ["db482bd8-e68d-3a38-e053-2995a90a38a5"], "pharm_class_epc": ["Histamine-2 Receptor Antagonist [EPC]"], "pharm_class_moa": ["Histamine H2 Receptor Antagonists [MoA]"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-697-51)", "package_ndc": "51655-697-51", "marketing_start_date": "20210401"}], "brand_name": "Cimetidine", "product_id": "51655-697_4950cd76-c47b-d0cf-e063-6394a90acf6d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H2 Receptor Antagonists [MoA]", "Histamine-2 Receptor Antagonist [EPC]"], "product_ndc": "51655-697", "generic_name": "cimetidine", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cimetidine", "active_ingredients": [{"name": "CIMETIDINE", "strength": "400 mg/1"}], "application_number": "ANDA074246", "marketing_category": "ANDA", "marketing_start_date": "20210401", "listing_expiration_date": "20271231"}