citalopram hydrobromide

Generic: citalopram hydrobromide

Labeler: advanced rx pharmacy of tennessee, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name citalopram hydrobromide
Generic Name citalopram hydrobromide
Labeler advanced rx pharmacy of tennessee, llc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

citalopram hydrobromide 10 mg/1

Manufacturer
Advanced Rx Pharmacy of Tennessee, LLC

Identifiers & Regulatory

Product NDC 80425-0309
Product ID 80425-0309_2a9bf621-afbd-7627-e063-6294a90a77a9
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077031
Listing Expiration 2026-12-31
Marketing Start 2023-04-06

Pharmacologic Class

Classes
serotonin reuptake inhibitor [epc] serotonin uptake inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 804250309
Hyphenated Format 80425-0309

Supplemental Identifiers

RxCUI
283672
UNII
I1E9D14F36

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 citalopram hydrobromide (source: ndc)
Generic Name citalopram hydrobromide (source: ndc)
Application Number ANDA077031 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (80425-0309-1)
  • 60 TABLET, FILM COATED in 1 BOTTLE (80425-0309-2)
  • 90 TABLET, FILM COATED in 1 BOTTLE (80425-0309-3)
source: ndc

Packages (3)

80425-0309-1 30 TABLET, FILM COATED in 1 BOTTLE (80425-0309-1) 80425-0309-2 60 TABLET, FILM COATED in 1 BOTTLE (80425-0309-2) 80425-0309-3 90 TABLET, FILM COATED in 1 BOTTLE (80425-0309-3)

Ingredients (1)

citalopram hydrobromide (10 mg/1)

Linked Drug Pages (1)

Citalopram Hydrobromide ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2a9bf621-afbd-7627-e063-6294a90a77a9", "openfda": {"unii": ["I1E9D14F36"], "rxcui": ["283672"], "spl_set_id": ["f8b06b55-f6a2-2438-e053-6394a90a530a"], "manufacturer_name": ["Advanced Rx Pharmacy of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (80425-0309-1)", "package_ndc": "80425-0309-1", "marketing_start_date": "20230406"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (80425-0309-2)", "package_ndc": "80425-0309-2", "marketing_start_date": "20230406"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (80425-0309-3)", "package_ndc": "80425-0309-3", "marketing_start_date": "20230406"}], "brand_name": "Citalopram Hydrobromide", "product_id": "80425-0309_2a9bf621-afbd-7627-e063-6294a90a77a9", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "80425-0309", "generic_name": "Citalopram Hydrobromide", "labeler_name": "Advanced Rx Pharmacy of Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Citalopram Hydrobromide", "active_ingredients": [{"name": "CITALOPRAM HYDROBROMIDE", "strength": "10 mg/1"}], "application_number": "ANDA077031", "marketing_category": "ANDA", "marketing_start_date": "20230406", "listing_expiration_date": "20261231"}