esomeprazole dr
Generic: esomeprazole dr
Labeler: direct_rxDrug Facts
Product Profile
Brand Name
esomeprazole dr
Generic Name
esomeprazole dr
Labeler
direct_rx
Dosage Form
CAPSULE, DELAYED RELEASE
Routes
Active Ingredients
esomeprazole magnesium 20 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
72189-381
Product ID
72189-381_2c4cbe6c-c27c-15fe-e063-6294a90ac409
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA211977
Listing Expiration
2026-12-31
Marketing Start
2022-09-13
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
72189381
Hyphenated Format
72189-381
Supplemental Identifiers
RxCUI
UNII
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
esomeprazole dr (source: ndc)
Generic Name
esomeprazole dr (source: ndc)
Application Number
ANDA211977 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/1
Packaging
- 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (72189-381-30)
- 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (72189-381-60)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2c4cbe6c-c27c-15fe-e063-6294a90ac409", "openfda": {"unii": ["R6DXU4WAY9"], "rxcui": ["606726"], "spl_set_id": ["e8937778-8baf-05f5-e053-2995a90a3a98"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (72189-381-30)", "package_ndc": "72189-381-30", "marketing_start_date": "20220913"}, {"sample": false, "description": "60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (72189-381-60)", "package_ndc": "72189-381-60", "marketing_start_date": "20220913"}], "brand_name": "Esomeprazole DR", "product_id": "72189-381_2c4cbe6c-c27c-15fe-e063-6294a90ac409", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Cytochrome P450 2C19 Inhibitors [MoA]", "Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "72189-381", "generic_name": "Esomeprazole DR", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Esomeprazole DR", "active_ingredients": [{"name": "ESOMEPRAZOLE MAGNESIUM", "strength": "20 mg/1"}], "application_number": "ANDA211977", "marketing_category": "ANDA", "marketing_start_date": "20220913", "listing_expiration_date": "20261231"}