citalopram hydrobromide

Generic: citalopram

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

Drug Facts

Product Profile

Brand Name citalopram hydrobromide
Generic Name citalopram
Labeler exelan pharmaceuticals inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

citalopram hydrobromide 20 mg/1

Manufacturer
Exelan Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 76282-629
Product ID 76282-629_fd69f24e-8108-4b9e-92ca-13ebbdf86e45
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077534
Listing Expiration 2026-12-31
Marketing Start 2017-11-10

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 76282629
Hyphenated Format 76282-629

Supplemental Identifiers

RxCUI
200371 283672 309314
UPC
0376282208909 0376282629902 0376282628905
UNII
I1E9D14F36

Packaging Origin

Original Packager
true

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 (source: ndc)
Application Number ANDA077534 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 500 TABLET in 1 BOTTLE (76282-629-05)
  • 1000 TABLET in 1 BOTTLE (76282-629-10)
  • 30 TABLET in 1 BOTTLE (76282-629-30)
  • 90 TABLET in 1 BOTTLE (76282-629-90)
source: ndc

Packages (4)

76282-629-05 500 TABLET in 1 BOTTLE (76282-629-05) 76282-629-10 1000 TABLET in 1 BOTTLE (76282-629-10) 76282-629-30 30 TABLET in 1 BOTTLE (76282-629-30) 76282-629-90 90 TABLET in 1 BOTTLE (76282-629-90)

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": "fd69f24e-8108-4b9e-92ca-13ebbdf86e45", "openfda": {"upc": ["0376282208909", "0376282629902", "0376282628905"], "unii": ["I1E9D14F36"], "rxcui": ["200371", "283672", "309314"], "spl_set_id": ["a8e8fde2-8392-4d5b-902b-e2b9dd55a02d"], "manufacturer_name": ["Exelan Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE (76282-629-05)", "package_ndc": "76282-629-05", "marketing_start_date": "20171110"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (76282-629-10)", "package_ndc": "76282-629-10", "marketing_start_date": "20171110"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (76282-629-30)", "package_ndc": "76282-629-30", "marketing_start_date": "20171110"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (76282-629-90)", "package_ndc": "76282-629-90", "marketing_start_date": "20171110"}], "brand_name": "CITALOPRAM HYDROBROMIDE", "product_id": "76282-629_fd69f24e-8108-4b9e-92ca-13ebbdf86e45", "dosage_form": "TABLET", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "76282-629", "generic_name": "CITALOPRAM", "labeler_name": "Exelan Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CITALOPRAM HYDROBROMIDE", "active_ingredients": [{"name": "CITALOPRAM HYDROBROMIDE", "strength": "20 mg/1"}], "application_number": "ANDA077534", "marketing_category": "ANDA", "marketing_start_date": "20171110", "listing_expiration_date": "20261231"}