citalopram

Generic: citalopram

Labeler: amneal pharmaceuticals llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name citalopram
Generic Name citalopram
Labeler amneal pharmaceuticals llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

citalopram hydrobromide 10 mg/1

Manufacturer
Amneal Pharmaceuticals LLC

Identifiers & Regulatory

Product NDC 65162-052
Product ID 65162-052_a42ab6f8-0664-4d9d-9da0-116bba7e55fc
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077289
Listing Expiration 2026-12-31
Marketing Start 2010-04-06

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 65162052
Hyphenated Format 65162-052

Supplemental Identifiers

RxCUI
200371 283672 309314
UPC
0365162053500 0365162054507 0365162052503
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 ANDA077289 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (65162-052-03)
  • 100 TABLET in 1 BOTTLE (65162-052-10)
  • 1000 TABLET in 1 BOTTLE (65162-052-11)
  • 500 TABLET in 1 BOTTLE (65162-052-50)
source: ndc

Packages (4)

65162-052-03 30 TABLET in 1 BOTTLE (65162-052-03) 65162-052-10 100 TABLET in 1 BOTTLE (65162-052-10) 65162-052-11 1000 TABLET in 1 BOTTLE (65162-052-11) 65162-052-50 500 TABLET in 1 BOTTLE (65162-052-50)

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": "a42ab6f8-0664-4d9d-9da0-116bba7e55fc", "openfda": {"upc": ["0365162053500", "0365162054507", "0365162052503"], "unii": ["I1E9D14F36"], "rxcui": ["200371", "283672", "309314"], "spl_set_id": ["6a402640-1c9d-4fca-8b5b-e1ac1dd4ca5a"], "manufacturer_name": ["Amneal Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (65162-052-03)", "package_ndc": "65162-052-03", "marketing_start_date": "20100406"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (65162-052-10)", "package_ndc": "65162-052-10", "marketing_start_date": "20100406"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (65162-052-11)", "package_ndc": "65162-052-11", "marketing_start_date": "20100406"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (65162-052-50)", "package_ndc": "65162-052-50", "marketing_start_date": "20100406"}], "brand_name": "Citalopram", "product_id": "65162-052_a42ab6f8-0664-4d9d-9da0-116bba7e55fc", "dosage_form": "TABLET", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "65162-052", "generic_name": "Citalopram", "labeler_name": "Amneal Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Citalopram", "active_ingredients": [{"name": "CITALOPRAM HYDROBROMIDE", "strength": "10 mg/1"}], "application_number": "ANDA077289", "marketing_category": "ANDA", "marketing_start_date": "20100406", "listing_expiration_date": "20261231"}