omeprazole

Generic: omeprazole

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name omeprazole
Generic Name omeprazole
Labeler proficient rx lp
Dosage Form CAPSULE, DELAYED RELEASE
Routes
ORAL
Active Ingredients

omeprazole 40 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 71205-157
Product ID 71205-157_9ee846e2-6191-4e7c-bdbe-86f868eecad6
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075410
Listing Expiration 2026-12-31
Marketing Start 2009-01-23

Pharmacologic Class

Established (EPC)
proton pump inhibitor [epc]
Mechanism of Action
proton pump inhibitors [moa] cytochrome p450 2c19 inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 71205157
Hyphenated Format 71205-157

Supplemental Identifiers

RxCUI
200329
UPC
0371205157609
UNII
KG60484QX9
NUI
N0000175525 N0000000147 N0000182140

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 ANDA075410 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 mg/1
source: ndc
Packaging
  • 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71205-157-30)
  • 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71205-157-60)
  • 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71205-157-90)
source: ndc

Packages (3)

71205-157-30 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71205-157-30) 71205-157-60 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71205-157-60) 71205-157-90 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71205-157-90)

Ingredients (1)

omeprazole (40 mg/1)

Linked Drug Pages (1)

Omeprazole ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "9ee846e2-6191-4e7c-bdbe-86f868eecad6", "openfda": {"nui": ["N0000175525", "N0000000147", "N0000182140"], "upc": ["0371205157609"], "unii": ["KG60484QX9"], "rxcui": ["200329"], "spl_set_id": ["9786b04f-f827-460b-91bc-c0ac967f95dd"], "pharm_class_epc": ["Proton Pump Inhibitor [EPC]"], "pharm_class_moa": ["Proton Pump Inhibitors [MoA]", "Cytochrome P450 2C19 Inhibitors [MoA]"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71205-157-30)", "package_ndc": "71205-157-30", "marketing_start_date": "20181101"}, {"sample": false, "description": "60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71205-157-60)", "package_ndc": "71205-157-60", "marketing_start_date": "20181101"}, {"sample": false, "description": "90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71205-157-90)", "package_ndc": "71205-157-90", "marketing_start_date": "20181101"}], "brand_name": "Omeprazole", "product_id": "71205-157_9ee846e2-6191-4e7c-bdbe-86f868eecad6", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Cytochrome P450 2C19 Inhibitors [MoA]", "Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "71205-157", "generic_name": "omeprazole", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Omeprazole", "active_ingredients": [{"name": "OMEPRAZOLE", "strength": "40 mg/1"}], "application_number": "ANDA075410", "marketing_category": "ANDA", "marketing_start_date": "20090123", "listing_expiration_date": "20261231"}