omeprazole
Generic: omeprazole
Labeler: sun pharmaceutical industries, inc.Drug Facts
Product Profile
Brand Name
omeprazole
Generic Name
omeprazole
Labeler
sun pharmaceutical industries, inc.
Dosage Form
TABLET, DELAYED RELEASE
Routes
Active Ingredients
omeprazole 20 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
62756-377
Product ID
62756-377_676e2f39-d83e-485a-9366-ed14c382e466
Product Type
HUMAN OTC DRUG
Marketing Category
ANDA
Application Number
ANDA207891
Listing Expiration
2026-12-31
Marketing Start
2019-01-01
Pharmacologic Class
Established (EPC)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
62756377
Hyphenated Format
62756-377
Supplemental Identifiers
RxCUI
UNII
NUI
Packaging Origin
Original Packager
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
ANDA207891 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/1
Packaging
- 2 BOTTLE in 1 CARTON (62756-377-11) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
- 3 BOTTLE in 1 CARTON (62756-377-12) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
- 1 BOTTLE in 1 CARTON (62756-377-21) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
- 1 BLISTER PACK in 1 CARTON (62756-377-70) / 14 TABLET, DELAYED RELEASE in 1 BLISTER PACK
- 3 BLISTER PACK in 1 CARTON (62756-377-79) / 14 TABLET, DELAYED RELEASE in 1 BLISTER PACK
- 2 BLISTER PACK in 1 CARTON (62756-377-96) / 14 TABLET, DELAYED RELEASE in 1 BLISTER PACK
Packages (6)
62756-377-11
2 BOTTLE in 1 CARTON (62756-377-11) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
62756-377-12
3 BOTTLE in 1 CARTON (62756-377-12) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
62756-377-21
1 BOTTLE in 1 CARTON (62756-377-21) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
62756-377-70
1 BLISTER PACK in 1 CARTON (62756-377-70) / 14 TABLET, DELAYED RELEASE in 1 BLISTER PACK
62756-377-79
3 BLISTER PACK in 1 CARTON (62756-377-79) / 14 TABLET, DELAYED RELEASE in 1 BLISTER PACK
62756-377-96
2 BLISTER PACK in 1 CARTON (62756-377-96) / 14 TABLET, DELAYED RELEASE in 1 BLISTER PACK
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "676e2f39-d83e-485a-9366-ed14c382e466", "openfda": {"nui": ["N0000175525", "N0000000147", "N0000182140"], "unii": ["KG60484QX9"], "rxcui": ["402014"], "spl_set_id": ["51c3ef34-b7c1-419e-a784-ae82540c7a22"], "pharm_class_epc": ["Proton Pump Inhibitor [EPC]"], "pharm_class_moa": ["Proton Pump Inhibitors [MoA]", "Cytochrome P450 2C19 Inhibitors [MoA]"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BOTTLE in 1 CARTON (62756-377-11) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE", "package_ndc": "62756-377-11", "marketing_start_date": "20190101"}, {"sample": false, "description": "3 BOTTLE in 1 CARTON (62756-377-12) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE", "package_ndc": "62756-377-12", "marketing_start_date": "20190101"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (62756-377-21) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE", "package_ndc": "62756-377-21", "marketing_start_date": "20190101"}, {"sample": false, "description": "1 BLISTER PACK in 1 CARTON (62756-377-70) / 14 TABLET, DELAYED RELEASE in 1 BLISTER PACK", "package_ndc": "62756-377-70", "marketing_start_date": "20190101"}, {"sample": false, "description": "3 BLISTER PACK in 1 CARTON (62756-377-79) / 14 TABLET, DELAYED RELEASE in 1 BLISTER PACK", "package_ndc": "62756-377-79", "marketing_start_date": "20190101"}, {"sample": false, "description": "2 BLISTER PACK in 1 CARTON (62756-377-96) / 14 TABLET, DELAYED RELEASE in 1 BLISTER PACK", "package_ndc": "62756-377-96", "marketing_start_date": "20190101"}], "brand_name": "Omeprazole", "product_id": "62756-377_676e2f39-d83e-485a-9366-ed14c382e466", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Cytochrome P450 2C19 Inhibitors [MoA]", "Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "62756-377", "generic_name": "Omeprazole", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Omeprazole", "active_ingredients": [{"name": "OMEPRAZOLE", "strength": "20 mg/1"}], "application_number": "ANDA207891", "marketing_category": "ANDA", "marketing_start_date": "20190101", "listing_expiration_date": "20261231"}