citalopram hydrobromide

Generic: citalopram hydrobromide

Labeler: quality care products, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name citalopram hydrobromide
Generic Name citalopram hydrobromide
Labeler quality care products, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

citalopram hydrobromide 20 mg/1

Manufacturer
Quality Care Products, LLC

Identifiers & Regulatory

Product NDC 55700-851
Product ID 55700-851_4e97913b-40ba-4158-a875-65496725b4e9
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078216
Marketing Start 2020-03-20
Marketing End 2026-10-31

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 55700851
Hyphenated Format 55700-851

Supplemental Identifiers

RxCUI
200371
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
  • 90 TABLET in 1 BOTTLE (55700-851-90)
source: ndc

Packages (1)

55700-851-90 90 TABLET in 1 BOTTLE (55700-851-90)

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": "4e97913b-40ba-4158-a875-65496725b4e9", "openfda": {"unii": ["I1E9D14F36"], "rxcui": ["200371"], "spl_set_id": ["6fc110ba-87e7-404e-9e00-b680f354c7b0"], "manufacturer_name": ["Quality Care Products, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (55700-851-90)", "package_ndc": "55700-851-90", "marketing_end_date": "20261031", "marketing_start_date": "20200820"}], "brand_name": "Citalopram Hydrobromide", "product_id": "55700-851_4e97913b-40ba-4158-a875-65496725b4e9", "dosage_form": "TABLET", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "55700-851", "generic_name": "Citalopram Hydrobromide", "labeler_name": "Quality Care Products, LLC", "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_end_date": "20261031", "marketing_start_date": "20200320"}