citalopram

Generic: citalopram hydrobromide

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

Drug Facts

Product Profile

Brand Name citalopram
Generic Name citalopram hydrobromide
Labeler aurobindo pharma limited
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

citalopram hydrobromide 40 mg/1

Manufacturer
Aurobindo Pharma Limited

Identifiers & Regulatory

Product NDC 65862-007
Product ID 65862-007_5642ea11-17b4-431a-a896-2cb336929100
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077031
Listing Expiration 2026-12-31
Marketing Start 2004-10-28

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 65862007
Hyphenated Format 65862-007

Supplemental Identifiers

RxCUI
200371 283672 309314
UPC
0365862007308 0365862006301 0365862005304
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 (source: ndc)
Generic Name citalopram hydrobromide (source: ndc)
Application Number ANDA077031 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (65862-007-01)
  • 500 TABLET, FILM COATED in 1 BOTTLE (65862-007-05)
  • 10 BLISTER PACK in 1 CARTON (65862-007-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK
  • 30 TABLET, FILM COATED in 1 BOTTLE (65862-007-30)
  • 30 TABLET, FILM COATED in 1 BLISTER PACK (65862-007-32)
  • 60 TABLET, FILM COATED in 1 BOTTLE (65862-007-60)
  • 90 TABLET, FILM COATED in 1 BOTTLE (65862-007-90)
source: ndc

Packages (7)

65862-007-01 100 TABLET, FILM COATED in 1 BOTTLE (65862-007-01) 65862-007-05 500 TABLET, FILM COATED in 1 BOTTLE (65862-007-05) 65862-007-10 10 BLISTER PACK in 1 CARTON (65862-007-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK 65862-007-30 30 TABLET, FILM COATED in 1 BOTTLE (65862-007-30) 65862-007-32 30 TABLET, FILM COATED in 1 BLISTER PACK (65862-007-32) 65862-007-60 60 TABLET, FILM COATED in 1 BOTTLE (65862-007-60) 65862-007-90 90 TABLET, FILM COATED in 1 BOTTLE (65862-007-90)

Ingredients (1)

citalopram hydrobromide (40 mg/1)

Linked Drug Pages (1)

Citalopram ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "5642ea11-17b4-431a-a896-2cb336929100", "openfda": {"upc": ["0365862007308", "0365862006301", "0365862005304"], "unii": ["I1E9D14F36"], "rxcui": ["200371", "283672", "309314"], "spl_set_id": ["2632b547-2e13-447f-ac85-c774e437d6a8"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (65862-007-01)", "package_ndc": "65862-007-01", "marketing_start_date": "20041028"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (65862-007-05)", "package_ndc": "65862-007-05", "marketing_start_date": "20041028"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (65862-007-10)  / 10 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "65862-007-10", "marketing_start_date": "20041028"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (65862-007-30)", "package_ndc": "65862-007-30", "marketing_start_date": "20041028"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (65862-007-32)", "package_ndc": "65862-007-32", "marketing_start_date": "20041028"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (65862-007-60)", "package_ndc": "65862-007-60", "marketing_start_date": "20041028"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (65862-007-90)", "package_ndc": "65862-007-90", "marketing_start_date": "20041028"}], "brand_name": "Citalopram", "product_id": "65862-007_5642ea11-17b4-431a-a896-2cb336929100", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "65862-007", "generic_name": "Citalopram Hydrobromide", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Citalopram", "active_ingredients": [{"name": "CITALOPRAM HYDROBROMIDE", "strength": "40 mg/1"}], "application_number": "ANDA077031", "marketing_category": "ANDA", "marketing_start_date": "20041028", "listing_expiration_date": "20261231"}