citalopram

Generic: citalopram hydrobromide

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

Drug Facts

Product Profile

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

citalopram hydrobromide 40 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 43063-670
Product ID 43063-670_413a0566-5adb-8c09-e063-6294a90a134e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077031
Listing Expiration 2026-12-31
Marketing Start 2004-10-28

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 43063670
Hyphenated Format 43063-670

Supplemental Identifiers

RxCUI
309314
UPC
0343063670903
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 hydrobromide (source: ndc)
Application Number ANDA077031 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-670-30)
  • 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-670-90)
source: ndc

Packages (2)

43063-670-30 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-670-30) 43063-670-90 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-670-90)

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": "413a0566-5adb-8c09-e063-6294a90a134e", "openfda": {"upc": ["0343063670903"], "unii": ["I1E9D14F36"], "rxcui": ["309314"], "spl_set_id": ["31a18cdf-b0aa-18f5-e054-00144ff8d46c"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-670-30)", "package_ndc": "43063-670-30", "marketing_start_date": "20160429"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-670-90)", "package_ndc": "43063-670-90", "marketing_start_date": "20160429"}], "brand_name": "Citalopram", "product_id": "43063-670_413a0566-5adb-8c09-e063-6294a90a134e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "43063-670", "generic_name": "Citalopram Hydrobromide", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Citalopram", "active_ingredients": [{"name": "CITALOPRAM HYDROBROMIDE", "strength": "40 mg/1"}], "application_number": "ANDA077031", "marketing_category": "ANDA", "marketing_start_date": "20041028", "listing_expiration_date": "20261231"}