citalopram hydrobromide

Generic: citalopram hydrobromide

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name citalopram hydrobromide
Generic Name citalopram hydrobromide
Labeler proficient rx lp
Dosage Form TABLET
Routes
ORAL
Active Ingredients

citalopram hydrobromide 20 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 63187-203
Product ID 63187-203_70196c8d-c1c0-457c-b9b2-dd1182416714
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 63187203
Hyphenated Format 63187-203

Supplemental Identifiers

RxCUI
200371 283672
UPC
0363187220303 0363187203900
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
  • 100 TABLET in 1 BOTTLE (63187-203-00)
  • 30 TABLET in 1 BOTTLE (63187-203-30)
  • 60 TABLET in 1 BOTTLE (63187-203-60)
  • 120 TABLET in 1 BOTTLE (63187-203-72)
  • 90 TABLET in 1 BOTTLE (63187-203-90)
source: ndc

Packages (5)

63187-203-00 100 TABLET in 1 BOTTLE (63187-203-00) 63187-203-30 30 TABLET in 1 BOTTLE (63187-203-30) 63187-203-60 60 TABLET in 1 BOTTLE (63187-203-60) 63187-203-72 120 TABLET in 1 BOTTLE (63187-203-72) 63187-203-90 90 TABLET in 1 BOTTLE (63187-203-90)

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": "70196c8d-c1c0-457c-b9b2-dd1182416714", "openfda": {"upc": ["0363187220303", "0363187203900"], "unii": ["I1E9D14F36"], "rxcui": ["200371", "283672"], "spl_set_id": ["1a136cc3-d655-4f3c-8710-2603dc008492"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (63187-203-00)", "package_ndc": "63187-203-00", "marketing_start_date": "20151102"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (63187-203-30)", "package_ndc": "63187-203-30", "marketing_start_date": "20151102"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (63187-203-60)", "package_ndc": "63187-203-60", "marketing_start_date": "20151102"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (63187-203-72)", "package_ndc": "63187-203-72", "marketing_start_date": "20151102"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (63187-203-90)", "package_ndc": "63187-203-90", "marketing_start_date": "20151102"}], "brand_name": "Citalopram Hydrobromide", "product_id": "63187-203_70196c8d-c1c0-457c-b9b2-dd1182416714", "dosage_form": "TABLET", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "63187-203", "generic_name": "Citalopram Hydrobromide", "labeler_name": "Proficient Rx LP", "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": "20071018", "listing_expiration_date": "20261231"}