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 20 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 43063-683
Product ID 43063-683_2fb360d2-ff23-9454-e063-6294a90ad2d0
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 43063683
Hyphenated Format 43063-683

Supplemental Identifiers

RxCUI
200371
UPC
0343063683309
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
  • 20 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-683-30)
  • 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-683-60)
  • 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-683-90)
source: ndc

Packages (3)

43063-683-30 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-683-30) 43063-683-60 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-683-60) 43063-683-90 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-683-90)

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": "2fb360d2-ff23-9454-e063-6294a90ad2d0", "openfda": {"upc": ["0343063683309"], "unii": ["I1E9D14F36"], "rxcui": ["200371"], "spl_set_id": ["43785b49-5d1e-4ae9-b2ff-26be910bde7f"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-683-30)", "package_ndc": "43063-683-30", "marketing_start_date": "20160624"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-683-60)", "package_ndc": "43063-683-60", "marketing_start_date": "20170915"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-683-90)", "package_ndc": "43063-683-90", "marketing_start_date": "20161025"}], "brand_name": "Citalopram", "product_id": "43063-683_2fb360d2-ff23-9454-e063-6294a90ad2d0", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "43063-683", "generic_name": "Citalopram", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Citalopram", "active_ingredients": [{"name": "CITALOPRAM HYDROBROMIDE", "strength": "20 mg/1"}], "application_number": "ANDA078216", "marketing_category": "ANDA", "marketing_start_date": "20071018", "listing_expiration_date": "20261231"}