citalopram hydrobromide

Generic: citalopram hydrobromide

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

Drug Facts

Product Profile

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

citalopram hydrobromide 20 mg/1

Manufacturer
Preferred Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 68788-0802
Product ID 68788-0802_543a6dbf-f42d-4bc1-ad77-9ceac5e6bfe9
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078216
Listing Expiration 2027-12-31
Marketing Start 2013-03-26

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 687880802
Hyphenated Format 68788-0802

Supplemental Identifiers

RxCUI
200371 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 hydrobromide (source: ndc)
Generic Name citalopram hydrobromide (source: ndc)
Application Number ANDA078216 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (68788-0802-1)
  • 30 TABLET, FILM COATED in 1 BOTTLE (68788-0802-3)
  • 60 TABLET, FILM COATED in 1 BOTTLE (68788-0802-6)
  • 120 TABLET, FILM COATED in 1 BOTTLE (68788-0802-8)
  • 90 TABLET, FILM COATED in 1 BOTTLE (68788-0802-9)
source: ndc

Packages (5)

68788-0802-1 100 TABLET, FILM COATED in 1 BOTTLE (68788-0802-1) 68788-0802-3 30 TABLET, FILM COATED in 1 BOTTLE (68788-0802-3) 68788-0802-6 60 TABLET, FILM COATED in 1 BOTTLE (68788-0802-6) 68788-0802-8 120 TABLET, FILM COATED in 1 BOTTLE (68788-0802-8) 68788-0802-9 90 TABLET, FILM COATED in 1 BOTTLE (68788-0802-9)

Ingredients (1)

citalopram hydrobromide (20 mg/1)

Linked Drug Pages (1)

Citalopram Hydrobromide ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "543a6dbf-f42d-4bc1-ad77-9ceac5e6bfe9", "openfda": {"unii": ["I1E9D14F36"], "rxcui": ["200371", "283672"], "spl_set_id": ["b52acd68-fed1-4680-9eaf-b72e7dcba6fb"], "manufacturer_name": ["Preferred Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (68788-0802-1)", "package_ndc": "68788-0802-1", "marketing_start_date": "20130326"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68788-0802-3)", "package_ndc": "68788-0802-3", "marketing_start_date": "20130326"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (68788-0802-6)", "package_ndc": "68788-0802-6", "marketing_start_date": "20130326"}, {"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE (68788-0802-8)", "package_ndc": "68788-0802-8", "marketing_start_date": "20130326"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (68788-0802-9)", "package_ndc": "68788-0802-9", "marketing_start_date": "20130326"}], "brand_name": "Citalopram Hydrobromide", "product_id": "68788-0802_543a6dbf-f42d-4bc1-ad77-9ceac5e6bfe9", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "68788-0802", "generic_name": "Citalopram Hydrobromide", "labeler_name": "Preferred Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Citalopram Hydrobromide", "active_ingredients": [{"name": "CITALOPRAM HYDROBROMIDE", "strength": "20 mg/1"}], "application_number": "ANDA078216", "marketing_category": "ANDA", "marketing_start_date": "20130326", "listing_expiration_date": "20271231"}