omeprazole
Generic: omeprazole
Labeler: a-s medication solutionsDrug Facts
Product Profile
Brand Name
omeprazole
Generic Name
omeprazole
Labeler
a-s medication solutions
Dosage Form
CAPSULE, DELAYED RELEASE
Routes
Active Ingredients
omeprazole 20 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
50090-3876
Product ID
50090-3876_bf1f317f-2f83-4725-915a-e59cc855ce2b
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA091672
Listing Expiration
2026-12-31
Marketing Start
2014-10-31
Pharmacologic Class
Established (EPC)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
500903876
Hyphenated Format
50090-3876
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
omeprazole (source: ndc)
Generic Name
omeprazole (source: ndc)
Application Number
ANDA091672 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/1
Packaging
- 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-3876-0)
- 15 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-3876-2)
- 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-3876-3)
- 20 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (50090-3876-4)
- 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-3876-5)
- 200 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-3876-6)
- 180 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-3876-7)
Packages (7)
50090-3876-0
30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-3876-0)
50090-3876-2
15 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-3876-2)
50090-3876-3
60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-3876-3)
50090-3876-4
20 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (50090-3876-4)
50090-3876-5
90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-3876-5)
50090-3876-6
200 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-3876-6)
50090-3876-7
180 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-3876-7)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "bf1f317f-2f83-4725-915a-e59cc855ce2b", "openfda": {"nui": ["N0000175525", "N0000000147", "N0000182140"], "unii": ["KG60484QX9"], "rxcui": ["198051"], "spl_set_id": ["5bda70ae-c3f6-450b-892f-6814795dd6ca"], "pharm_class_epc": ["Proton Pump Inhibitor [EPC]"], "pharm_class_moa": ["Proton Pump Inhibitors [MoA]", "Cytochrome P450 2C19 Inhibitors [MoA]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-3876-0)", "package_ndc": "50090-3876-0", "marketing_start_date": "20181128"}, {"sample": false, "description": "15 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-3876-2)", "package_ndc": "50090-3876-2", "marketing_start_date": "20181128"}, {"sample": false, "description": "60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-3876-3)", "package_ndc": "50090-3876-3", "marketing_start_date": "20181128"}, {"sample": false, "description": "20 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (50090-3876-4)", "package_ndc": "50090-3876-4", "marketing_start_date": "20141128"}, {"sample": false, "description": "90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-3876-5)", "package_ndc": "50090-3876-5", "marketing_start_date": "20181128"}, {"sample": false, "description": "200 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-3876-6)", "package_ndc": "50090-3876-6", "marketing_start_date": "20181128"}, {"sample": false, "description": "180 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-3876-7)", "package_ndc": "50090-3876-7", "marketing_start_date": "20181128"}], "brand_name": "Omeprazole", "product_id": "50090-3876_bf1f317f-2f83-4725-915a-e59cc855ce2b", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Cytochrome P450 2C19 Inhibitors [MoA]", "Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "50090-3876", "generic_name": "Omeprazole", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Omeprazole", "active_ingredients": [{"name": "OMEPRAZOLE", "strength": "20 mg/1"}], "application_number": "ANDA091672", "marketing_category": "ANDA", "marketing_start_date": "20141031", "listing_expiration_date": "20261231"}