acid reducer

Generic: omeprazole

Labeler: aurohealth llc
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name acid reducer
Generic Name omeprazole
Labeler aurohealth llc
Dosage Form TABLET, DELAYED RELEASE
Routes
ORAL
Active Ingredients

omeprazole magnesium 20 mg/1

Manufacturer
Aurohealth LLC

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
cytochrome p450 2c19 inhibitors [moa] proton pump inhibitor [epc] proton pump inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 58602729
Hyphenated Format 58602-729

Supplemental Identifiers

RxCUI
402014
UPC
0358602729059
UNII
426QFE7XLK

Packaging Origin

Original Packager
true

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
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
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)
source: ndc

Packages (7)

Ingredients (1)

omeprazole magnesium (20 mg/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"}