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
Routes
ORAL
Active Ingredients

citalopram hydrobromide 10 mg/1

Manufacturer
St Marys Medical Park Pharmacy

Identifiers & Regulatory

Product NDC 60760-009
Product ID 60760-009_ded44f64-c51c-1454-e053-2995a90a908c
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 60760009
Hyphenated Format 60760-009

Supplemental Identifiers

RxCUI
283672
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
  • 10 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE, PLASTIC (60760-009-30)
  • 90 TABLET in 1 BOTTLE, PLASTIC (60760-009-90)
source: ndc

Packages (2)

60760-009-30 30 TABLET in 1 BOTTLE, PLASTIC (60760-009-30) 60760-009-90 90 TABLET in 1 BOTTLE, PLASTIC (60760-009-90)

Ingredients (1)

citalopram hydrobromide (10 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": "ded44f64-c51c-1454-e053-2995a90a908c", "openfda": {"unii": ["I1E9D14F36"], "rxcui": ["283672"], "spl_set_id": ["351ca54b-0eb6-4e93-8ab4-82fb18dcc9e1"], "manufacturer_name": ["St Marys Medical Park Pharmacy"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (60760-009-30)", "package_ndc": "60760-009-30", "marketing_start_date": "20071018"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (60760-009-90)", "package_ndc": "60760-009-90", "marketing_start_date": "20071018"}], "brand_name": "Citalopram Hydrobromide", "product_id": "60760-009_ded44f64-c51c-1454-e053-2995a90a908c", "dosage_form": "TABLET", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "60760-009", "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": "10 mg/1"}], "application_number": "ANDA078216", "marketing_category": "ANDA", "marketing_start_date": "20071018", "listing_expiration_date": "20261231"}