citalopram

Generic: citalopram

Labeler: pd-rx pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

citalopram hydrobromide 10 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 43063-481
Product ID 43063-481_2f361594-eb68-f951-e063-6294a90a5006
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078216
Listing Expiration 2026-12-31
Marketing Start 2007-10-18

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 43063481
Hyphenated Format 43063-481

Supplemental Identifiers

RxCUI
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
  • 5 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-481-05)
  • 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-481-30)
source: ndc

Packages (2)

43063-481-05 5 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-481-05) 43063-481-30 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-481-30)

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": "2f361594-eb68-f951-e063-6294a90a5006", "openfda": {"unii": ["I1E9D14F36"], "rxcui": ["283672"], "spl_set_id": ["df929b3f-0cda-4a75-96d3-22e6b0edbbc9"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "5 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-481-05)", "package_ndc": "43063-481-05", "marketing_start_date": "20150403"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-481-30)", "package_ndc": "43063-481-30", "marketing_start_date": "20161027"}], "brand_name": "Citalopram", "product_id": "43063-481_2f361594-eb68-f951-e063-6294a90a5006", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "43063-481", "generic_name": "Citalopram", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "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": "20071018", "listing_expiration_date": "20261231"}