omeprazole
Generic: omeprazole
Labeler: pd-rx pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
omeprazole
Generic Name
omeprazole
Labeler
pd-rx pharmaceuticals, inc.
Dosage Form
CAPSULE, DELAYED RELEASE
Routes
Active Ingredients
omeprazole 40 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
72789-257
Product ID
72789-257_4bac7b98-8e95-1e51-e063-6294a90ab1cc
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA078490
Listing Expiration
2027-12-31
Marketing Start
2014-03-01
Pharmacologic Class
Established (EPC)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
72789257
Hyphenated Format
72789-257
Supplemental Identifiers
RxCUI
UPC
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
ANDA078490 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 40 mg/1
Packaging
- 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (72789-257-90)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4bac7b98-8e95-1e51-e063-6294a90ab1cc", "openfda": {"nui": ["N0000175525", "N0000000147", "N0000182140"], "upc": ["0372789257907"], "unii": ["KG60484QX9"], "rxcui": ["200329"], "spl_set_id": ["0344268f-d8e6-48d5-b1e1-f750ed1d8a52"], "pharm_class_epc": ["Proton Pump Inhibitor [EPC]"], "pharm_class_moa": ["Proton Pump Inhibitors [MoA]", "Cytochrome P450 2C19 Inhibitors [MoA]"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (72789-257-90)", "package_ndc": "72789-257-90", "marketing_start_date": "20220705"}], "brand_name": "Omeprazole", "product_id": "72789-257_4bac7b98-8e95-1e51-e063-6294a90ab1cc", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Cytochrome P450 2C19 Inhibitors [MoA]", "Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "72789-257", "generic_name": "Omeprazole", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Omeprazole", "active_ingredients": [{"name": "OMEPRAZOLE", "strength": "40 mg/1"}], "application_number": "ANDA078490", "marketing_category": "ANDA", "marketing_start_date": "20140301", "listing_expiration_date": "20271231"}