citalopram
Generic: citalopram
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
citalopram
Generic Name
citalopram
Labeler
bryant ranch prepack
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
citalopram hydrobromide 40 mg/1
Manufacturer
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
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
713352232
Hyphenated Format
71335-2232
Supplemental Identifiers
RxCUI
UNII
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
source: ndc
Resolved Composition
Strengths
- 40 mg/1
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)
Packages (6)
71335-2232-1
30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2232-1)
71335-2232-2
40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2232-2)
71335-2232-3
60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2232-3)
71335-2232-4
90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2232-4)
71335-2232-5
100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2232-5)
71335-2232-6
180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2232-6)
Ingredients (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"}