citalopram

Generic: citalopram

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name citalopram
Generic Name citalopram
Labeler bryant ranch prepack
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

citalopram hydrobromide 40 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-2232
Product ID 71335-2232_ff4ddb77-91cf-4e45-b855-55e4c264d085
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077042
Listing Expiration 2026-12-31
Marketing Start 2008-07-28

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 713352232
Hyphenated Format 71335-2232

Supplemental Identifiers

RxCUI
309314
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 (source: ndc)
Generic Name citalopram (source: ndc)
Application Number ANDA077042 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2232-1)
  • 40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2232-2)
  • 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2232-3)
  • 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2232-4)
  • 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2232-5)
  • 180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2232-6)
source: ndc

Packages (6)

Ingredients (1)

citalopram hydrobromide (40 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "ff4ddb77-91cf-4e45-b855-55e4c264d085", "openfda": {"unii": ["I1E9D14F36"], "rxcui": ["309314"], "spl_set_id": ["2a8acad8-0ba0-4631-9f6d-f587e7a8558c"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2232-1)", "package_ndc": "71335-2232-1", "marketing_start_date": "20230918"}, {"sample": false, "description": "40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2232-2)", "package_ndc": "71335-2232-2", "marketing_start_date": "20241004"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2232-3)", "package_ndc": "71335-2232-3", "marketing_start_date": "20241004"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2232-4)", "package_ndc": "71335-2232-4", "marketing_start_date": "20230918"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2232-5)", "package_ndc": "71335-2232-5", "marketing_start_date": "20241004"}, {"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2232-6)", "package_ndc": "71335-2232-6", "marketing_start_date": "20241004"}], "brand_name": "Citalopram", "product_id": "71335-2232_ff4ddb77-91cf-4e45-b855-55e4c264d085", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "71335-2232", "generic_name": "citalopram", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Citalopram", "active_ingredients": [{"name": "CITALOPRAM HYDROBROMIDE", "strength": "40 mg/1"}], "application_number": "ANDA077042", "marketing_category": "ANDA", "marketing_start_date": "20080728", "listing_expiration_date": "20261231"}