citalopram

Generic: citalopram hydrobromide

Labeler: nucare pharmaceuticals,inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

citalopram hydrobromide 40 mg/1

Manufacturer
NuCare Pharmaceuticals,Inc.

Identifiers & Regulatory

Product NDC 68071-3357
Product ID 68071-3357_3880e5dd-0433-2990-e063-6394a90a0ef8
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 680713357
Hyphenated Format 68071-3357

Supplemental Identifiers

RxCUI
309314
UPC
0368071335798
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
  • 15 TABLET, FILM COATED in 1 BOTTLE (68071-3357-1)
  • 30 TABLET, FILM COATED in 1 BOTTLE (68071-3357-3)
  • 40 TABLET, FILM COATED in 1 BOTTLE (68071-3357-4)
  • 45 TABLET, FILM COATED in 1 BOTTLE (68071-3357-5)
  • 60 TABLET, FILM COATED in 1 BOTTLE (68071-3357-6)
  • 90 TABLET, FILM COATED in 1 BOTTLE (68071-3357-9)
source: ndc

Packages (6)

68071-3357-1 15 TABLET, FILM COATED in 1 BOTTLE (68071-3357-1) 68071-3357-3 30 TABLET, FILM COATED in 1 BOTTLE (68071-3357-3) 68071-3357-4 40 TABLET, FILM COATED in 1 BOTTLE (68071-3357-4) 68071-3357-5 45 TABLET, FILM COATED in 1 BOTTLE (68071-3357-5) 68071-3357-6 60 TABLET, FILM COATED in 1 BOTTLE (68071-3357-6) 68071-3357-9 90 TABLET, FILM COATED in 1 BOTTLE (68071-3357-9)

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": "3880e5dd-0433-2990-e063-6394a90a0ef8", "openfda": {"upc": ["0368071335798"], "unii": ["I1E9D14F36"], "rxcui": ["309314"], "spl_set_id": ["544ba802-a536-579a-e054-00144ff88e88"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "15 TABLET, FILM COATED in 1 BOTTLE (68071-3357-1)", "package_ndc": "68071-3357-1", "marketing_start_date": "20170714"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68071-3357-3)", "package_ndc": "68071-3357-3", "marketing_start_date": "20170714"}, {"sample": false, "description": "40 TABLET, FILM COATED in 1 BOTTLE (68071-3357-4)", "package_ndc": "68071-3357-4", "marketing_start_date": "20170714"}, {"sample": false, "description": "45 TABLET, FILM COATED in 1 BOTTLE (68071-3357-5)", "package_ndc": "68071-3357-5", "marketing_start_date": "20170714"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (68071-3357-6)", "package_ndc": "68071-3357-6", "marketing_start_date": "20170714"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (68071-3357-9)", "package_ndc": "68071-3357-9", "marketing_start_date": "20170714"}], "brand_name": "Citalopram", "product_id": "68071-3357_3880e5dd-0433-2990-e063-6394a90a0ef8", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "68071-3357", "generic_name": "Citalopram Hydrobromide", "labeler_name": "NuCare 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"}