citalopram hydrobromide

Generic: citalopram hydrobromide

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

Drug Facts

Product Profile

Brand Name citalopram hydrobromide
Generic Name citalopram hydrobromide
Labeler bryant ranch prepack
Dosage Form TABLET
Routes
ORAL
Active Ingredients

citalopram hydrobromide 40 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-0480
Product ID 71335-0480_fc40aa2f-2477-4703-8749-cd7b8e8d4323
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078216
Listing Expiration 2026-12-31
Marketing Start 2007-10-18

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 713350480
Hyphenated Format 71335-0480

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 hydrobromide (source: ndc)
Generic Name citalopram hydrobromide (source: ndc)
Application Number ANDA078216 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (71335-0480-1)
  • 40 TABLET in 1 BOTTLE (71335-0480-2)
  • 60 TABLET in 1 BOTTLE (71335-0480-3)
  • 90 TABLET in 1 BOTTLE (71335-0480-4)
  • 100 TABLET in 1 BOTTLE (71335-0480-5)
  • 180 TABLET in 1 BOTTLE (71335-0480-6)
source: ndc

Packages (6)

71335-0480-1 30 TABLET in 1 BOTTLE (71335-0480-1) 71335-0480-2 40 TABLET in 1 BOTTLE (71335-0480-2) 71335-0480-3 60 TABLET in 1 BOTTLE (71335-0480-3) 71335-0480-4 90 TABLET in 1 BOTTLE (71335-0480-4) 71335-0480-5 100 TABLET in 1 BOTTLE (71335-0480-5) 71335-0480-6 180 TABLET in 1 BOTTLE (71335-0480-6)

Ingredients (1)

citalopram hydrobromide (40 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": "fc40aa2f-2477-4703-8749-cd7b8e8d4323", "openfda": {"unii": ["I1E9D14F36"], "rxcui": ["309314"], "spl_set_id": ["15cb00da-4435-4930-90d0-faadf2739a5c"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-0480-1)", "package_ndc": "71335-0480-1", "marketing_start_date": "20180226"}, {"sample": false, "description": "40 TABLET in 1 BOTTLE (71335-0480-2)", "package_ndc": "71335-0480-2", "marketing_start_date": "20241030"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-0480-3)", "package_ndc": "71335-0480-3", "marketing_start_date": "20180426"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-0480-4)", "package_ndc": "71335-0480-4", "marketing_start_date": "20180222"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (71335-0480-5)", "package_ndc": "71335-0480-5", "marketing_start_date": "20191111"}, {"sample": false, "description": "180 TABLET in 1 BOTTLE (71335-0480-6)", "package_ndc": "71335-0480-6", "marketing_start_date": "20230810"}], "brand_name": "Citalopram Hydrobromide", "product_id": "71335-0480_fc40aa2f-2477-4703-8749-cd7b8e8d4323", "dosage_form": "TABLET", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "71335-0480", "generic_name": "Citalopram Hydrobromide", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Citalopram Hydrobromide", "active_ingredients": [{"name": "CITALOPRAM HYDROBROMIDE", "strength": "40 mg/1"}], "application_number": "ANDA078216", "marketing_category": "ANDA", "marketing_start_date": "20071018", "listing_expiration_date": "20261231"}