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Drug Facts
Distributed by McKesson Corp.,
via Strategic Sourcing Services LLC,
Memphis, TN 38141
The following Structured Product Label (SPL) was submitted to the FDA by Strategic Sourcing Services for the product Omeprazole (NDC 70677-0148). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding other, active ingredient (in each tablet), purpose, use, warnings, do not use if you have, ask a docotor befor use if you have, ask a doctor or pharmacist before use if you are, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Drug Facts
Distributed by McKesson Corp.,
via Strategic Sourcing Services LLC,
Memphis, TN 38141
Omeprazole USP 20 mg
Acid reducer
Allergy alert: Do not use if you are allergic to omeprazole.
These may be signs of a serious condition. See your doctor.
taking a prescription drug. Acid reducers may interact with certain prescription drugs.
If pregnant or breast-feeding, ask a health professional before use.
In case of overdose, get medical help or contact a Poison Control Center right away. (1-800-222-1222).
14-Day Course of Treatment
Repeated 14-Day Courses (if needed)
anhydrous lactose, hypromellose, hypromellose acetate succinate, iron oxide red, iron oxide yellow, lactose monohydrate, methyl cellulose, monoethanolamine, propylene glycol, sodium lauryl sulfate, sodium starch glycolate, sodium stearate, sodium stearyl fumarate, talc, titanium dioxide and triethyl citrate.
The imprinting ink contains ammonium hydroxide, black iron oxide, n-butyl alcohol, propylene glycol and shellac.
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