citalopram hydrobromide

Generic: citalopram hydrobromide

Labeler: st marys medical park pharmacy
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name citalopram hydrobromide
Generic Name citalopram hydrobromide
Labeler st marys medical park pharmacy
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

citalopram hydrobromide 20 mg/1

Manufacturer
St Marys Medical Park Pharmacy

Identifiers & Regulatory

Product NDC 60760-495
Product ID 60760-495_364689f2-275d-3160-e063-6394a90a0ce0
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078216
Listing Expiration 2026-12-31
Marketing Start 2014-01-23

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 60760495
Hyphenated Format 60760-495

Supplemental Identifiers

RxCUI
200371
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
  • 20 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-495-30)
source: ndc

Packages (1)

60760-495-30 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-495-30)

Ingredients (1)

citalopram hydrobromide (20 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": "364689f2-275d-3160-e063-6394a90a0ce0", "openfda": {"unii": ["I1E9D14F36"], "rxcui": ["200371"], "spl_set_id": ["db900453-4777-4142-a236-5d3a6152d0a5"], "manufacturer_name": ["St Marys Medical Park Pharmacy"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-495-30)", "package_ndc": "60760-495-30", "marketing_start_date": "20250529"}], "brand_name": "Citalopram Hydrobromide", "product_id": "60760-495_364689f2-275d-3160-e063-6394a90a0ce0", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "60760-495", "generic_name": "Citalopram Hydrobromide", "labeler_name": "St Marys Medical Park Pharmacy", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Citalopram Hydrobromide", "active_ingredients": [{"name": "CITALOPRAM HYDROBROMIDE", "strength": "20 mg/1"}], "application_number": "ANDA078216", "marketing_category": "ANDA", "marketing_start_date": "20140123", "listing_expiration_date": "20261231"}