citalopram

Generic: citalopram

Labeler: mylan pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name citalopram
Generic Name citalopram
Labeler mylan pharmaceuticals inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

citalopram hydrobromide 20 mg/1

Manufacturer
Mylan Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 0378-6232
Product ID 0378-6232_55e0b75b-3772-4f5b-a162-1f70719daf3d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077042
Listing Expiration 2026-12-31
Marketing Start 2008-07-28

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 03786232
Hyphenated Format 0378-6232

Supplemental Identifiers

RxCUI
200371 283672 309314
UPC
0303786232017 0303786231010 0303786233014
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 ANDA077042 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-6232-01)
  • 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-6232-05)
source: ndc

Packages (2)

0378-6232-01 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-6232-01) 0378-6232-05 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-6232-05)

Ingredients (1)

citalopram hydrobromide (20 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": "55e0b75b-3772-4f5b-a162-1f70719daf3d", "openfda": {"upc": ["0303786232017", "0303786231010", "0303786233014"], "unii": ["I1E9D14F36"], "rxcui": ["200371", "283672", "309314"], "spl_set_id": ["825c0c49-5fbf-6d8b-cb8c-94ebf0eda043"], "manufacturer_name": ["Mylan Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-6232-01)", "package_ndc": "0378-6232-01", "marketing_start_date": "20080728"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-6232-05)", "package_ndc": "0378-6232-05", "marketing_start_date": "20080728"}], "brand_name": "Citalopram", "product_id": "0378-6232_55e0b75b-3772-4f5b-a162-1f70719daf3d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "0378-6232", "generic_name": "citalopram", "labeler_name": "Mylan Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Citalopram", "active_ingredients": [{"name": "CITALOPRAM HYDROBROMIDE", "strength": "20 mg/1"}], "application_number": "ANDA077042", "marketing_category": "ANDA", "marketing_start_date": "20080728", "listing_expiration_date": "20261231"}