escitalopram oral solution
Generic: escitalopram oral
Labeler: chartwell governmental & specialty rx, llc.Drug Facts
Product Profile
Brand Name
escitalopram oral solution
Generic Name
escitalopram oral
Labeler
chartwell governmental & specialty rx, llc.
Dosage Form
SOLUTION
Routes
Active Ingredients
escitalopram oxalate 5 mg/5mL
Manufacturer
Identifiers & Regulatory
Product NDC
68999-729
Product ID
68999-729_499eac58-9e20-d82d-e063-6294a90a6b46
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA090477
Listing Expiration
2027-12-31
Marketing Start
2023-06-12
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
68999729
Hyphenated Format
68999-729
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
escitalopram oral solution (source: ndc)
Generic Name
escitalopram oral (source: ndc)
Application Number
ANDA090477 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 5 mg/5mL
Packaging
- 2 TRAY in 1 BOX (68999-729-24) / 10 CUP in 1 TRAY / 10 mL in 1 CUP (68999-729-10)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "499eac58-9e20-d82d-e063-6294a90a6b46", "openfda": {"unii": ["5U85DBW7LO"], "rxcui": ["351285"], "spl_set_id": ["45ed4d16-6358-40a1-9352-319e58f55e5d"], "manufacturer_name": ["Chartwell Governmental & Specialty RX, LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 TRAY in 1 BOX (68999-729-24) / 10 CUP in 1 TRAY / 10 mL in 1 CUP (68999-729-10)", "package_ndc": "68999-729-24", "marketing_start_date": "20260121"}], "brand_name": "Escitalopram Oral Solution", "product_id": "68999-729_499eac58-9e20-d82d-e063-6294a90a6b46", "dosage_form": "SOLUTION", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "68999-729", "generic_name": "Escitalopram Oral", "labeler_name": "Chartwell Governmental & Specialty RX, LLC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Escitalopram Oral Solution", "active_ingredients": [{"name": "ESCITALOPRAM OXALATE", "strength": "5 mg/5mL"}], "application_number": "ANDA090477", "marketing_category": "ANDA", "marketing_start_date": "20230612", "listing_expiration_date": "20271231"}