citalopram

Generic: citalopram

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

Drug Facts

Product Profile

Brand Name citalopram
Generic Name citalopram
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 68071-3558
Product ID 68071-3558_0dfb11d9-f48e-56ee-e063-6294a90ad256
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077042
Listing Expiration 2026-12-31
Marketing Start 2008-07-28

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 680713558
Hyphenated Format 68071-3558

Supplemental Identifiers

RxCUI
309314
UPC
0368071355819
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 ANDA077042 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68071-3558-1)
source: ndc

Packages (1)

68071-3558-1 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68071-3558-1)

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": "0dfb11d9-f48e-56ee-e063-6294a90ad256", "openfda": {"upc": ["0368071355819"], "unii": ["I1E9D14F36"], "rxcui": ["309314"], "spl_set_id": ["0dfb11d9-f48d-56ee-e063-6294a90ad256"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68071-3558-1)", "package_ndc": "68071-3558-1", "marketing_start_date": "20240102"}], "brand_name": "Citalopram", "product_id": "68071-3558_0dfb11d9-f48e-56ee-e063-6294a90ad256", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "68071-3558", "generic_name": "citalopram", "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": "ANDA077042", "marketing_category": "ANDA", "marketing_start_date": "20080728", "listing_expiration_date": "20261231"}