citalopram hydrobromide
Generic: citalopram hydrobromide
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
citalopram hydrobromide
Generic Name
citalopram hydrobromide
Labeler
bryant ranch prepack
Dosage Form
TABLET
Routes
Active Ingredients
citalopram hydrobromide 10 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
71335-0377
Product ID
71335-0377_b53065df-1ffb-4d72-b9b0-733e1c7be862
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA078216
Listing Expiration
2026-12-31
Marketing Start
2007-10-18
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
713350377
Hyphenated Format
71335-0377
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 hydrobromide (source: ndc)
Generic Name
citalopram hydrobromide (source: ndc)
Application Number
ANDA078216 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/1
Packaging
- 30 TABLET in 1 BOTTLE (71335-0377-1)
- 60 TABLET in 1 BOTTLE (71335-0377-2)
- 90 TABLET in 1 BOTTLE (71335-0377-3)
- 21 TABLET in 1 BOTTLE (71335-0377-4)
Packages (4)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "b53065df-1ffb-4d72-b9b0-733e1c7be862", "openfda": {"unii": ["I1E9D14F36"], "rxcui": ["283672"], "spl_set_id": ["9b53c14c-224c-49ed-8a00-96f871593ab0"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-0377-1)", "package_ndc": "71335-0377-1", "marketing_start_date": "20180212"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-0377-2)", "package_ndc": "71335-0377-2", "marketing_start_date": "20180427"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-0377-3)", "package_ndc": "71335-0377-3", "marketing_start_date": "20180322"}, {"sample": false, "description": "21 TABLET in 1 BOTTLE (71335-0377-4)", "package_ndc": "71335-0377-4", "marketing_start_date": "20241030"}], "brand_name": "Citalopram Hydrobromide", "product_id": "71335-0377_b53065df-1ffb-4d72-b9b0-733e1c7be862", "dosage_form": "TABLET", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "71335-0377", "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": "10 mg/1"}], "application_number": "ANDA078216", "marketing_category": "ANDA", "marketing_start_date": "20071018", "listing_expiration_date": "20261231"}