citalopram hydrobromide

Generic: citalopram hydrobromide

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

Drug Facts

Product Profile

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

citalopram hydrobromide 20 mg/1

Manufacturer
NuCare Pharmaceuticals,Inc.

Identifiers & Regulatory

Product NDC 68071-5132
Product ID 68071-5132_1b54ac75-c339-ac54-e063-6294a90af1d3
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 680715132
Hyphenated Format 68071-5132

Supplemental Identifiers

RxCUI
200371
UPC
0368071513233
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
  • 30 TABLET in 1 BOTTLE (68071-5132-3)
source: ndc

Packages (1)

68071-5132-3 30 TABLET in 1 BOTTLE (68071-5132-3)

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": "1b54ac75-c339-ac54-e063-6294a90af1d3", "openfda": {"upc": ["0368071513233"], "unii": ["I1E9D14F36"], "rxcui": ["200371"], "spl_set_id": ["9987a273-e6d7-54cd-e053-2a95a90a0aaa"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68071-5132-3)", "package_ndc": "68071-5132-3", "marketing_start_date": "20191212"}], "brand_name": "Citalopram Hydrobromide", "product_id": "68071-5132_1b54ac75-c339-ac54-e063-6294a90af1d3", "dosage_form": "TABLET", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "68071-5132", "generic_name": "Citalopram Hydrobromide", "labeler_name": "NuCare 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": "20071018", "listing_expiration_date": "20261231"}