omeprazole magnesium
Generic: omeprazole magnesium
Labeler: hebDrug Facts
Product Profile
Brand Name
omeprazole magnesium
Generic Name
omeprazole magnesium
Labeler
heb
Dosage Form
CAPSULE, DELAYED RELEASE
Routes
Active Ingredients
omeprazole magnesium 20 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
37808-006
Product ID
37808-006_22f3dce6-c417-c720-8fb1-b45a46321c4a
Product Type
HUMAN OTC DRUG
Marketing Category
ANDA
Application Number
ANDA078878
Listing Expiration
2026-12-31
Marketing Start
2016-01-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
37808006
Hyphenated Format
37808-006
Supplemental Identifiers
RxCUI
UNII
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 magnesium (source: ndc)
Generic Name
omeprazole magnesium (source: ndc)
Application Number
ANDA078878 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/1
Packaging
- 3 BOTTLE in 1 CARTON (37808-006-33) / 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE
- 1 BOTTLE in 1 CARTON (37808-006-52) / 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "22f3dce6-c417-c720-8fb1-b45a46321c4a", "openfda": {"unii": ["426QFE7XLK"], "rxcui": ["198051"], "spl_set_id": ["5d8b3f5f-f680-64ae-b360-c0bd06b2ac92"], "manufacturer_name": ["HEB"]}, "finished": true, "packaging": [{"sample": false, "description": "3 BOTTLE in 1 CARTON (37808-006-33) / 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE", "package_ndc": "37808-006-33", "marketing_start_date": "20160101"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (37808-006-52) / 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE", "package_ndc": "37808-006-52", "marketing_start_date": "20160101"}], "brand_name": "Omeprazole Magnesium", "product_id": "37808-006_22f3dce6-c417-c720-8fb1-b45a46321c4a", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Cytochrome P450 2C19 Inhibitors [MoA]", "Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "37808-006", "generic_name": "Omeprazole Magnesium", "labeler_name": "HEB", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Omeprazole Magnesium", "active_ingredients": [{"name": "OMEPRAZOLE MAGNESIUM", "strength": "20 mg/1"}], "application_number": "ANDA078878", "marketing_category": "ANDA", "marketing_start_date": "20160101", "listing_expiration_date": "20261231"}