citalopram

Generic: citalopram

Labeler: major pharmaceuticals
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

citalopram hydrobromide 10 mg/1

Manufacturer
Major Pharmaceuticals

Identifiers & Regulatory

Product NDC 0904-6084
Product ID 0904-6084_5bf8d853-5669-4ef2-940e-6c9075a45ce9
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078216
Listing Expiration 2027-12-31
Marketing Start 2009-11-02

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 09046084
Hyphenated Format 0904-6084

Supplemental Identifiers

RxCUI
200371 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 (source: ndc)
Generic Name citalopram (source: ndc)
Application Number ANDA078216 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 100 BLISTER PACK in 1 CARTON (0904-6084-61) / 1 TABLET, FILM COATED in 1 BLISTER PACK
source: ndc

Packages (1)

0904-6084-61 100 BLISTER PACK in 1 CARTON (0904-6084-61) / 1 TABLET, FILM COATED in 1 BLISTER PACK

Ingredients (1)

citalopram hydrobromide (10 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": "5bf8d853-5669-4ef2-940e-6c9075a45ce9", "openfda": {"unii": ["I1E9D14F36"], "rxcui": ["200371", "283672"], "spl_set_id": ["a6949652-b15b-435b-9097-2219f398ac05"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0904-6084-61)  / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "0904-6084-61", "marketing_start_date": "20091102"}], "brand_name": "Citalopram", "product_id": "0904-6084_5bf8d853-5669-4ef2-940e-6c9075a45ce9", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "0904-6084", "generic_name": "Citalopram", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Citalopram", "active_ingredients": [{"name": "CITALOPRAM HYDROBROMIDE", "strength": "10 mg/1"}], "application_number": "ANDA078216", "marketing_category": "ANDA", "marketing_start_date": "20091102", "listing_expiration_date": "20271231"}