citalopram

Generic: citalopram

Labeler: cipla usa inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name citalopram
Generic Name citalopram
Labeler cipla usa inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

citalopram hydrobromide 20 mg/1

Manufacturer
Cipla USA Inc.

Identifiers & Regulatory

Product NDC 69097-823
Product ID 69097-823_6f82cb3c-dec1-4200-9cfa-9b41438a71b8
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077534
Listing Expiration 2026-12-31
Marketing Start 2016-07-22

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 69097823
Hyphenated Format 69097-823

Supplemental Identifiers

RxCUI
200371 283672 309314
UPC
0369097822071 0369097823122 0369097824075 0369097823078
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 (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
  • 30 TABLET in 1 BOTTLE (69097-823-02)
  • 100 TABLET in 1 BOTTLE (69097-823-07)
  • 500 TABLET in 1 BOTTLE (69097-823-12)
  • 1000 TABLET in 1 BOTTLE (69097-823-15)
source: ndc

Packages (4)

69097-823-02 30 TABLET in 1 BOTTLE (69097-823-02) 69097-823-07 100 TABLET in 1 BOTTLE (69097-823-07) 69097-823-12 500 TABLET in 1 BOTTLE (69097-823-12) 69097-823-15 1000 TABLET in 1 BOTTLE (69097-823-15)

Ingredients (1)

citalopram hydrobromide (20 mg/1)

Linked Drug Pages (1)

Citalopram ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "6f82cb3c-dec1-4200-9cfa-9b41438a71b8", "openfda": {"upc": ["0369097822071", "0369097823122", "0369097824075", "0369097823078"], "unii": ["I1E9D14F36"], "rxcui": ["200371", "283672", "309314"], "spl_set_id": ["0580559a-783a-4a0a-8d81-ee30a29077c5"], "manufacturer_name": ["Cipla USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (69097-823-02)", "package_ndc": "69097-823-02", "marketing_start_date": "20160722"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (69097-823-07)", "package_ndc": "69097-823-07", "marketing_start_date": "20160722"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (69097-823-12)", "package_ndc": "69097-823-12", "marketing_start_date": "20160722"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (69097-823-15)", "package_ndc": "69097-823-15", "marketing_start_date": "20160722"}], "brand_name": "Citalopram", "product_id": "69097-823_6f82cb3c-dec1-4200-9cfa-9b41438a71b8", "dosage_form": "TABLET", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "69097-823", "generic_name": "Citalopram", "labeler_name": "Cipla USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Citalopram", "active_ingredients": [{"name": "CITALOPRAM HYDROBROMIDE", "strength": "20 mg/1"}], "application_number": "ANDA077534", "marketing_category": "ANDA", "marketing_start_date": "20160722", "listing_expiration_date": "20261231"}