citalopram

Generic: citalopram

Labeler: torrent pharmaceuticals limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name citalopram
Generic Name citalopram
Labeler torrent pharmaceuticals limited
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

citalopram hydrobromide 20 mg/1

Manufacturer
Torrent Pharmaceuticals Limited

Identifiers & Regulatory

Product NDC 13668-010
Product ID 13668-010_48423caf-4df2-4653-a8ed-b28462757ed3
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078216
Listing Expiration 2027-12-31
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 13668010
Hyphenated Format 13668-010

Supplemental Identifiers

RxCUI
200371 283672 309314
UPC
0313668010015 0313668011012
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 ANDA078216 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (13668-010-01)
  • 500 TABLET, FILM COATED in 1 BOTTLE (13668-010-05)
  • 5600 TABLET, FILM COATED in 1 BOTTLE (13668-010-06)
  • 30 TABLET, FILM COATED in 1 BOTTLE (13668-010-30)
source: ndc

Packages (4)

13668-010-01 100 TABLET, FILM COATED in 1 BOTTLE (13668-010-01) 13668-010-05 500 TABLET, FILM COATED in 1 BOTTLE (13668-010-05) 13668-010-06 5600 TABLET, FILM COATED in 1 BOTTLE (13668-010-06) 13668-010-30 30 TABLET, FILM COATED in 1 BOTTLE (13668-010-30)

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": "48423caf-4df2-4653-a8ed-b28462757ed3", "openfda": {"upc": ["0313668010015", "0313668011012"], "unii": ["I1E9D14F36"], "rxcui": ["200371", "283672", "309314"], "spl_set_id": ["04766f1d-7a69-49ed-8fd3-1a6305505d47"], "manufacturer_name": ["Torrent Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (13668-010-01)", "package_ndc": "13668-010-01", "marketing_start_date": "20071018"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (13668-010-05)", "package_ndc": "13668-010-05", "marketing_start_date": "20071018"}, {"sample": false, "description": "5600 TABLET, FILM COATED in 1 BOTTLE (13668-010-06)", "package_ndc": "13668-010-06", "marketing_start_date": "20071018"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (13668-010-30)", "package_ndc": "13668-010-30", "marketing_start_date": "20071018"}], "brand_name": "Citalopram", "product_id": "13668-010_48423caf-4df2-4653-a8ed-b28462757ed3", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "13668-010", "generic_name": "Citalopram", "labeler_name": "Torrent Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Citalopram", "active_ingredients": [{"name": "CITALOPRAM HYDROBROMIDE", "strength": "20 mg/1"}], "application_number": "ANDA078216", "marketing_category": "ANDA", "marketing_start_date": "20071018", "listing_expiration_date": "20271231"}