citalopram hydrobromide

Generic: citalopram hydrobromide

Labeler: aurobindo pharma limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name citalopram hydrobromide
Generic Name citalopram hydrobromide
Labeler aurobindo pharma limited
Dosage Form SOLUTION
Routes
ORAL
Active Ingredients

citalopram hydrobromide 10 mg/5mL

Manufacturer
Aurobindo Pharma Limited

Identifiers & Regulatory

Product NDC 65862-074
Product ID 65862-074_7cecadcf-9da0-41e4-b9fd-0fe04572dcd8
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077812
Listing Expiration 2026-12-31
Marketing Start 2006-08-28

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 65862074
Hyphenated Format 65862-074

Supplemental Identifiers

RxCUI
309313
UNII
I1E9D14F36

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 citalopram hydrobromide (source: ndc)
Generic Name citalopram hydrobromide (source: ndc)
Application Number ANDA077812 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/5mL
source: ndc
Packaging
  • 240 mL in 1 BOTTLE (65862-074-24)
source: ndc

Packages (1)

65862-074-24 240 mL in 1 BOTTLE (65862-074-24)

Ingredients (1)

citalopram hydrobromide (10 mg/5mL)

Linked Drug Pages (1)

Citalopram Hydrobromide ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "7cecadcf-9da0-41e4-b9fd-0fe04572dcd8", "openfda": {"unii": ["I1E9D14F36"], "rxcui": ["309313"], "spl_set_id": ["e7a2cbdd-1bdb-4e59-a3dd-298a189753ae"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "240 mL in 1 BOTTLE (65862-074-24)", "package_ndc": "65862-074-24", "marketing_start_date": "20060828"}], "brand_name": "Citalopram Hydrobromide", "product_id": "65862-074_7cecadcf-9da0-41e4-b9fd-0fe04572dcd8", "dosage_form": "SOLUTION", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "65862-074", "generic_name": "Citalopram Hydrobromide", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Citalopram Hydrobromide", "active_ingredients": [{"name": "CITALOPRAM HYDROBROMIDE", "strength": "10 mg/5mL"}], "application_number": "ANDA077812", "marketing_category": "ANDA", "marketing_start_date": "20060828", "listing_expiration_date": "20261231"}