citalopram

Generic: citalopram

Labeler: pd-rx pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name citalopram
Generic Name citalopram
Labeler pd-rx pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

citalopram hydrobromide 20 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 43063-063
Product ID 43063-063_2b24d618-2b9f-f54e-e063-6394a90a9c46
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077289
Listing Expiration 2026-12-31
Marketing Start 2010-04-06

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 43063063
Hyphenated Format 43063-063

Supplemental Identifiers

RxCUI
200371
UPC
0343063221013
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 (source: ndc)
Generic Name citalopram (source: ndc)
Application Number ANDA077289 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 14 TABLET in 1 BOTTLE, PLASTIC (43063-063-14)
  • 30 TABLET in 1 BOTTLE, PLASTIC (43063-063-30)
  • 60 TABLET in 1 BOTTLE, PLASTIC (43063-063-60)
  • 90 TABLET in 1 BOTTLE, PLASTIC (43063-063-90)
source: ndc

Packages (4)

43063-063-14 14 TABLET in 1 BOTTLE, PLASTIC (43063-063-14) 43063-063-30 30 TABLET in 1 BOTTLE, PLASTIC (43063-063-30) 43063-063-60 60 TABLET in 1 BOTTLE, PLASTIC (43063-063-60) 43063-063-90 90 TABLET in 1 BOTTLE, PLASTIC (43063-063-90)

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": "2b24d618-2b9f-f54e-e063-6394a90a9c46", "openfda": {"upc": ["0343063221013"], "unii": ["I1E9D14F36"], "rxcui": ["200371"], "spl_set_id": ["75f6db65-e4ed-470a-9e56-12791f22ee9b"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "14 TABLET in 1 BOTTLE, PLASTIC (43063-063-14)", "package_ndc": "43063-063-14", "marketing_start_date": "20120821"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (43063-063-30)", "package_ndc": "43063-063-30", "marketing_start_date": "20120821"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (43063-063-60)", "package_ndc": "43063-063-60", "marketing_start_date": "20120821"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (43063-063-90)", "package_ndc": "43063-063-90", "marketing_start_date": "20120821"}], "brand_name": "Citalopram", "product_id": "43063-063_2b24d618-2b9f-f54e-e063-6394a90a9c46", "dosage_form": "TABLET", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "43063-063", "generic_name": "Citalopram", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Citalopram", "active_ingredients": [{"name": "CITALOPRAM HYDROBROMIDE", "strength": "20 mg/1"}], "application_number": "ANDA077289", "marketing_category": "ANDA", "marketing_start_date": "20100406", "listing_expiration_date": "20261231"}