acid reducer
Generic: omeprazole
Labeler: aurohealth llcDrug Facts
Product Profile
Brand Name
acid reducer
Generic Name
omeprazole
Labeler
aurohealth llc
Dosage Form
TABLET, DELAYED RELEASE
Routes
Active Ingredients
omeprazole magnesium 20 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
58602-729
Product ID
58602-729_81d45120-49d4-4de8-8477-79312e2c1d56
Product Type
HUMAN OTC DRUG
Marketing Category
ANDA
Application Number
ANDA206877
Listing Expiration
2026-12-31
Marketing Start
2018-06-06
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
58602729
Hyphenated Format
58602-729
Supplemental Identifiers
RxCUI
UPC
UNII
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
acid reducer (source: ndc)
Generic Name
omeprazole (source: ndc)
Application Number
ANDA206877 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/1
Packaging
- 1 BLISTER PACK in 1 CARTON (58602-729-01) / 14 TABLET, DELAYED RELEASE in 1 BLISTER PACK
- 2 BLISTER PACK in 1 CARTON (58602-729-02) / 14 TABLET, DELAYED RELEASE in 1 BLISTER PACK
- 3 BLISTER PACK in 1 CARTON (58602-729-03) / 14 TABLET, DELAYED RELEASE in 1 BLISTER PACK
- 1 BOTTLE in 1 CARTON (58602-729-05) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
- 2 BOTTLE in 1 CARTON (58602-729-61) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
- 3 BOTTLE in 1 CARTON (58602-729-62) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
- 2 BLISTER PACK in 1 CARTON (58602-729-65) / 7 TABLET, DELAYED RELEASE in 1 BLISTER PACK (58602-729-64)
Packages (7)
58602-729-01
1 BLISTER PACK in 1 CARTON (58602-729-01) / 14 TABLET, DELAYED RELEASE in 1 BLISTER PACK
58602-729-02
2 BLISTER PACK in 1 CARTON (58602-729-02) / 14 TABLET, DELAYED RELEASE in 1 BLISTER PACK
58602-729-03
3 BLISTER PACK in 1 CARTON (58602-729-03) / 14 TABLET, DELAYED RELEASE in 1 BLISTER PACK
58602-729-05
1 BOTTLE in 1 CARTON (58602-729-05) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
58602-729-61
2 BOTTLE in 1 CARTON (58602-729-61) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
58602-729-62
3 BOTTLE in 1 CARTON (58602-729-62) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
58602-729-65
2 BLISTER PACK in 1 CARTON (58602-729-65) / 7 TABLET, DELAYED RELEASE in 1 BLISTER PACK (58602-729-64)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "81d45120-49d4-4de8-8477-79312e2c1d56", "openfda": {"upc": ["0358602729059"], "unii": ["426QFE7XLK"], "rxcui": ["402014"], "spl_set_id": ["fde12bf8-3e3b-4813-a8c4-4385e7de8204"], "manufacturer_name": ["Aurohealth LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (58602-729-01) / 14 TABLET, DELAYED RELEASE in 1 BLISTER PACK", "package_ndc": "58602-729-01", "marketing_start_date": "20180606"}, {"sample": false, "description": "2 BLISTER PACK in 1 CARTON (58602-729-02) / 14 TABLET, DELAYED RELEASE in 1 BLISTER PACK", "package_ndc": "58602-729-02", "marketing_start_date": "20180606"}, {"sample": false, "description": "3 BLISTER PACK in 1 CARTON (58602-729-03) / 14 TABLET, DELAYED RELEASE in 1 BLISTER PACK", "package_ndc": "58602-729-03", "marketing_start_date": "20180606"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (58602-729-05) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE", "package_ndc": "58602-729-05", "marketing_start_date": "20180606"}, {"sample": false, "description": "2 BOTTLE in 1 CARTON (58602-729-61) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE", "package_ndc": "58602-729-61", "marketing_start_date": "20180606"}, {"sample": false, "description": "3 BOTTLE in 1 CARTON (58602-729-62) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE", "package_ndc": "58602-729-62", "marketing_start_date": "20180606"}, {"sample": false, "description": "2 BLISTER PACK in 1 CARTON (58602-729-65) / 7 TABLET, DELAYED RELEASE in 1 BLISTER PACK (58602-729-64)", "package_ndc": "58602-729-65", "marketing_start_date": "20180606"}], "brand_name": "Acid Reducer", "product_id": "58602-729_81d45120-49d4-4de8-8477-79312e2c1d56", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Cytochrome P450 2C19 Inhibitors [MoA]", "Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "58602-729", "generic_name": "Omeprazole", "labeler_name": "Aurohealth LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Acid Reducer", "active_ingredients": [{"name": "OMEPRAZOLE MAGNESIUM", "strength": "20 mg/1"}], "application_number": "ANDA206877", "marketing_category": "ANDA", "marketing_start_date": "20180606", "listing_expiration_date": "20261231"}