citalopram

Generic: citalopram

Labeler: chartwell governmental & specialty rx, llc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name citalopram
Generic Name citalopram
Labeler chartwell governmental & specialty rx, llc.
Dosage Form SOLUTION
Routes
ORAL
Active Ingredients

citalopram hydrobromide 10 mg/5mL

Manufacturer
Chartwell Governmental & Specialty RX, LLC.

Identifiers & Regulatory

Product NDC 68999-540
Product ID 68999-540_484c3f19-d5f7-3e00-e063-6394a90a1938
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077629
Listing Expiration 2027-12-31
Marketing Start 2006-06-14

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 68999540
Hyphenated Format 68999-540

Supplemental Identifiers

RxCUI
309313
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 ANDA077629 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/5mL
source: ndc
Packaging
  • 2 TRAY in 1 BOX (68999-540-24) / 10 CUP in 1 TRAY / 10 mL in 1 CUP (68999-540-10)
source: ndc

Packages (1)

Ingredients (1)

citalopram hydrobromide (10 mg/5mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "484c3f19-d5f7-3e00-e063-6394a90a1938", "openfda": {"unii": ["I1E9D14F36"], "rxcui": ["309313"], "spl_set_id": ["3114274f-d81f-4b1f-8f17-35db9eee2ffe"], "manufacturer_name": ["Chartwell Governmental & Specialty RX, LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 TRAY in 1 BOX (68999-540-24)  / 10 CUP in 1 TRAY / 10 mL in 1 CUP (68999-540-10)", "package_ndc": "68999-540-24", "marketing_start_date": "20260113"}], "brand_name": "Citalopram", "product_id": "68999-540_484c3f19-d5f7-3e00-e063-6394a90a1938", "dosage_form": "SOLUTION", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "68999-540", "generic_name": "Citalopram", "labeler_name": "Chartwell Governmental & Specialty RX, LLC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Citalopram", "active_ingredients": [{"name": "CITALOPRAM HYDROBROMIDE", "strength": "10 mg/5mL"}], "application_number": "ANDA077629", "marketing_category": "ANDA", "marketing_start_date": "20060614", "listing_expiration_date": "20271231"}