naproxen and esomeprazole magnesium
Generic: naproxen and esomeprazole magnesium
Labeler: asclemed usa, inc.Drug Facts
Product Profile
Brand Name
naproxen and esomeprazole magnesium
Generic Name
naproxen and esomeprazole magnesium
Labeler
asclemed usa, inc.
Dosage Form
TABLET, DELAYED RELEASE
Routes
Active Ingredients
esomeprazole magnesium 20 mg/1, naproxen 375 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
76420-890
Product ID
76420-890_2a4fb535-ba1a-05d6-e063-6394a90a0b29
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA204206
Listing Expiration
2026-12-31
Marketing Start
2020-02-18
Pharmacologic Class
Established (EPC)
Mechanism of Action
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
76420890
Hyphenated Format
76420-890
Supplemental Identifiers
RxCUI
UNII
NUI
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
naproxen and esomeprazole magnesium (source: ndc)
Generic Name
naproxen and esomeprazole magnesium (source: ndc)
Application Number
ANDA204206 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/1
- 375 mg/1
Packaging
- 100 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-890-01)
- 30 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-890-30)
- 60 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-890-60)
- 90 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-890-90)
Packages (4)
Ingredients (2)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2a4fb535-ba1a-05d6-e063-6394a90a0b29", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["57Y76R9ATQ", "R6DXU4WAY9"], "rxcui": ["994005", "994008"], "spl_set_id": ["7b3af5a8-0c92-43f4-af13-7a47dca20e92"], "pharm_class_cs": ["Anti-Inflammatory Agents, Non-Steroidal [CS]"], "pharm_class_epc": ["Nonsteroidal Anti-inflammatory Drug [EPC]"], "pharm_class_moa": ["Cyclooxygenase Inhibitors [MoA]"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-890-01)", "package_ndc": "76420-890-01", "marketing_start_date": "20241228"}, {"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-890-30)", "package_ndc": "76420-890-30", "marketing_start_date": "20241228"}, {"sample": false, "description": "60 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-890-60)", "package_ndc": "76420-890-60", "marketing_start_date": "20241228"}, {"sample": false, "description": "90 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-890-90)", "package_ndc": "76420-890-90", "marketing_start_date": "20241228"}], "brand_name": "Naproxen and esomeprazole magnesium", "product_id": "76420-890_2a4fb535-ba1a-05d6-e063-6394a90a0b29", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Cytochrome P450 2C19 Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]", "Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "76420-890", "generic_name": "Naproxen and esomeprazole magnesium", "labeler_name": "Asclemed USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Naproxen and esomeprazole magnesium", "active_ingredients": [{"name": "ESOMEPRAZOLE MAGNESIUM", "strength": "20 mg/1"}, {"name": "NAPROXEN", "strength": "375 mg/1"}], "application_number": "ANDA204206", "marketing_category": "ANDA", "marketing_start_date": "20200218", "listing_expiration_date": "20261231"}