citalopram

Generic: citalopram

Labeler: northwind health company, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name citalopram
Generic Name citalopram
Labeler northwind health company, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

citalopram hydrobromide 40 mg/1

Manufacturer
Northwind Health Company, LLC

Identifiers & Regulatory

Product NDC 51655-209
Product ID 51655-209_48d2a0a2-f269-ef1d-e063-6394a90a49c2
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077534
Listing Expiration 2027-12-31
Marketing Start 2022-10-21

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 51655209
Hyphenated Format 51655-209

Supplemental Identifiers

RxCUI
309314
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 ANDA077534 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 mg/1
source: ndc
Packaging
  • 90 TABLET in 1 BOTTLE, PLASTIC (51655-209-26)
  • 30 TABLET in 1 BOTTLE, PLASTIC (51655-209-52)
source: ndc

Packages (2)

51655-209-26 90 TABLET in 1 BOTTLE, PLASTIC (51655-209-26) 51655-209-52 30 TABLET in 1 BOTTLE, PLASTIC (51655-209-52)

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": "48d2a0a2-f269-ef1d-e063-6394a90a49c2", "openfda": {"unii": ["I1E9D14F36"], "rxcui": ["309314"], "spl_set_id": ["f2b54f10-221f-5eed-e053-2995a90ab47f"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (51655-209-26)", "package_ndc": "51655-209-26", "marketing_start_date": "20221021"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (51655-209-52)", "package_ndc": "51655-209-52", "marketing_start_date": "20230103"}], "brand_name": "Citalopram", "product_id": "51655-209_48d2a0a2-f269-ef1d-e063-6394a90a49c2", "dosage_form": "TABLET", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "51655-209", "generic_name": "Citalopram", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Citalopram", "active_ingredients": [{"name": "CITALOPRAM HYDROBROMIDE", "strength": "40 mg/1"}], "application_number": "ANDA077534", "marketing_category": "ANDA", "marketing_start_date": "20221021", "listing_expiration_date": "20271231"}