cimetidine

Generic: cimetidine

Labeler: chartwell rx, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name cimetidine
Generic Name cimetidine
Labeler chartwell rx, llc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

cimetidine 200 mg/1

Manufacturer
Chartwell RX, LLC

Identifiers & Regulatory

Product NDC 62135-630
Product ID 62135-630_0337689b-c5d5-d881-e063-6394a90aaec9
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA074329
Listing Expiration 2026-12-31
Marketing Start 1994-05-17

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 62135630
Hyphenated Format 62135-630

Supplemental Identifiers

RxCUI
197505 197506 197507 197508
UPC
0362135633905 0362135630300 0362135631901 0362135632908
UNII
80061L1WGD
NUI
N0000000151 N0000175784

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 cimetidine (source: ndc)
Generic Name cimetidine (source: ndc)
Application Number ANDA074329 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 200 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (62135-630-30)
source: ndc

Packages (1)

62135-630-30 30 TABLET, FILM COATED in 1 BOTTLE (62135-630-30)

Ingredients (1)

cimetidine (200 mg/1)

Linked Drug Pages (1)

CIMETIDINE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "0337689b-c5d5-d881-e063-6394a90aaec9", "openfda": {"nui": ["N0000000151", "N0000175784"], "upc": ["0362135633905", "0362135630300", "0362135631901", "0362135632908"], "unii": ["80061L1WGD"], "rxcui": ["197505", "197506", "197507", "197508"], "spl_set_id": ["01997826-7ca1-473e-bfc9-075b14b58a35"], "pharm_class_epc": ["Histamine-2 Receptor Antagonist [EPC]"], "pharm_class_moa": ["Histamine H2 Receptor Antagonists [MoA]"], "manufacturer_name": ["Chartwell RX, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (62135-630-30)", "package_ndc": "62135-630-30", "marketing_start_date": "20230815"}], "brand_name": "CIMETIDINE", "product_id": "62135-630_0337689b-c5d5-d881-e063-6394a90aaec9", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H2 Receptor Antagonists [MoA]", "Histamine-2 Receptor Antagonist [EPC]"], "product_ndc": "62135-630", "generic_name": "CIMETIDINE", "labeler_name": "Chartwell RX, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CIMETIDINE", "active_ingredients": [{"name": "CIMETIDINE", "strength": "200 mg/1"}], "application_number": "ANDA074329", "marketing_category": "ANDA", "marketing_start_date": "19940517", "listing_expiration_date": "20261231"}