omeprazole
Generic: omeprazole
Labeler: preferred pharmaceuticals inc.Drug Facts
Product Profile
Brand Name
omeprazole
Generic Name
omeprazole
Labeler
preferred pharmaceuticals inc.
Dosage Form
CAPSULE, DELAYED RELEASE
Routes
Active Ingredients
omeprazole 20 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
68788-6881
Product ID
68788-6881_2ab7deaf-58ca-47ce-97ea-17adaf9d5d15
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA091672
Listing Expiration
2026-12-31
Marketing Start
2017-01-20
Pharmacologic Class
Established (EPC)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
687886881
Hyphenated Format
68788-6881
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
- 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-6881-1)
- 20 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-6881-2)
- 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-6881-3)
- 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-6881-4)
- 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-6881-6)
- 120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-6881-8)
- 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-6881-9)
Packages (7)
68788-6881-1
100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-6881-1)
68788-6881-2
20 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-6881-2)
68788-6881-3
30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-6881-3)
68788-6881-4
14 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-6881-4)
68788-6881-6
60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-6881-6)
68788-6881-8
120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-6881-8)
68788-6881-9
90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-6881-9)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2ab7deaf-58ca-47ce-97ea-17adaf9d5d15", "openfda": {"nui": ["N0000175525", "N0000000147", "N0000182140"], "unii": ["KG60484QX9"], "rxcui": ["198051"], "spl_set_id": ["aa8fc2ea-3942-453b-bc19-1e4b14ba6926"], "pharm_class_epc": ["Proton Pump Inhibitor [EPC]"], "pharm_class_moa": ["Proton Pump Inhibitors [MoA]", "Cytochrome P450 2C19 Inhibitors [MoA]"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-6881-1)", "package_ndc": "68788-6881-1", "marketing_start_date": "20170120"}, {"sample": false, "description": "20 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-6881-2)", "package_ndc": "68788-6881-2", "marketing_start_date": "20170120"}, {"sample": false, "description": "30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-6881-3)", "package_ndc": "68788-6881-3", "marketing_start_date": "20170120"}, {"sample": false, "description": "14 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-6881-4)", "package_ndc": "68788-6881-4", "marketing_start_date": "20170120"}, {"sample": false, "description": "60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-6881-6)", "package_ndc": "68788-6881-6", "marketing_start_date": "20170120"}, {"sample": false, "description": "120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-6881-8)", "package_ndc": "68788-6881-8", "marketing_start_date": "20170120"}, {"sample": false, "description": "90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-6881-9)", "package_ndc": "68788-6881-9", "marketing_start_date": "20170120"}], "brand_name": "Omeprazole", "product_id": "68788-6881_2ab7deaf-58ca-47ce-97ea-17adaf9d5d15", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Cytochrome P450 2C19 Inhibitors [MoA]", "Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "68788-6881", "generic_name": "Omeprazole", "labeler_name": "Preferred Pharmaceuticals Inc.", "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": "20170120", "listing_expiration_date": "20261231"}