citalopram

Generic: citalopram

Labeler: epic pharma, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name citalopram
Generic Name citalopram
Labeler epic pharma, llc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

citalopram hydrobromide 40 mg/1

Manufacturer
Epic Pharma, LLC

Identifiers & Regulatory

Product NDC 42806-021
Product ID 42806-021_b7f54932-2c8c-44f4-acc6-d9e2b3914be9
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077045
Listing Expiration 2026-12-31
Marketing Start 2011-05-20

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 42806021
Hyphenated Format 42806-021

Supplemental Identifiers

RxCUI
200371 283672 309314
UPC
0342806019306 0342806020012
UNII
I1E9D14F36

Packaging Origin

Original Packager
true

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 (source: ndc)
Generic Name citalopram (source: ndc)
Application Number ANDA077045 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (42806-021-01)
  • 1000 TABLET, FILM COATED in 1 BOTTLE (42806-021-10)
  • 30 TABLET, FILM COATED in 1 BOTTLE (42806-021-30)
source: ndc

Packages (3)

42806-021-01 100 TABLET, FILM COATED in 1 BOTTLE (42806-021-01) 42806-021-10 1000 TABLET, FILM COATED in 1 BOTTLE (42806-021-10) 42806-021-30 30 TABLET, FILM COATED in 1 BOTTLE (42806-021-30)

Ingredients (1)

citalopram hydrobromide (40 mg/1)

Linked Drug Pages (1)

CITALOPRAM ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "b7f54932-2c8c-44f4-acc6-d9e2b3914be9", "openfda": {"upc": ["0342806019306", "0342806020012"], "unii": ["I1E9D14F36"], "rxcui": ["200371", "283672", "309314"], "spl_set_id": ["08b6d5da-5919-4760-9e16-3b478a14d6d7"], "manufacturer_name": ["Epic Pharma, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (42806-021-01)", "package_ndc": "42806-021-01", "marketing_start_date": "20110520"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (42806-021-10)", "package_ndc": "42806-021-10", "marketing_start_date": "20110520"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (42806-021-30)", "package_ndc": "42806-021-30", "marketing_start_date": "20110520"}], "brand_name": "CITALOPRAM", "product_id": "42806-021_b7f54932-2c8c-44f4-acc6-d9e2b3914be9", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "42806-021", "generic_name": "citalopram", "labeler_name": "Epic Pharma, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CITALOPRAM", "active_ingredients": [{"name": "CITALOPRAM HYDROBROMIDE", "strength": "40 mg/1"}], "application_number": "ANDA077045", "marketing_category": "ANDA", "marketing_start_date": "20110520", "listing_expiration_date": "20261231"}