citalopram hydrobromide

Generic: citalopram hydrobromide

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name citalopram hydrobromide
Generic Name citalopram hydrobromide
Labeler a-s medication solutions
Dosage Form TABLET
Routes
ORAL
Active Ingredients

citalopram hydrobromide 40 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-3208
Product ID 50090-3208_62db333a-b8cc-414a-b4c2-18bceabb8691
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078216
Listing Expiration 2026-12-31
Marketing Start 2007-10-18

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500903208
Hyphenated Format 50090-3208

Supplemental Identifiers

RxCUI
200371 283672 309314
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
  • 40 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (50090-3208-0)
  • 100 TABLET in 1 BOTTLE (50090-3208-1)
  • 90 TABLET in 1 BOTTLE (50090-3208-2)
source: ndc

Packages (3)

50090-3208-0 30 TABLET in 1 BOTTLE (50090-3208-0) 50090-3208-1 100 TABLET in 1 BOTTLE (50090-3208-1) 50090-3208-2 90 TABLET in 1 BOTTLE (50090-3208-2)

Ingredients (1)

citalopram hydrobromide (40 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": "62db333a-b8cc-414a-b4c2-18bceabb8691", "openfda": {"unii": ["I1E9D14F36"], "rxcui": ["200371", "283672", "309314"], "spl_set_id": ["05421bee-f746-418e-bb9c-ab44a89b567d"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-3208-0)", "package_ndc": "50090-3208-0", "marketing_start_date": "20171024"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (50090-3208-1)", "package_ndc": "50090-3208-1", "marketing_start_date": "20171026"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-3208-2)", "package_ndc": "50090-3208-2", "marketing_start_date": "20171024"}], "brand_name": "Citalopram Hydrobromide", "product_id": "50090-3208_62db333a-b8cc-414a-b4c2-18bceabb8691", "dosage_form": "TABLET", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "50090-3208", "generic_name": "Citalopram Hydrobromide", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Citalopram Hydrobromide", "active_ingredients": [{"name": "CITALOPRAM HYDROBROMIDE", "strength": "40 mg/1"}], "application_number": "ANDA078216", "marketing_category": "ANDA", "marketing_start_date": "20071018", "listing_expiration_date": "20261231"}