Omeprazole Delayed Release Tablets 20 mg

Manufacturer
MARKSANS PHARMA LIMITED
Effective date
2025-08-11
Label type
Human OTC Drug Label
Version
3
Source
full-release
Hydrated at
2026-06-01 01:09:58

Label at a glance#

ProductOmeprazole 20 mg
Active ingredientOMEPRAZOLE MAGNESIUM
Label structure15 sections

Dosage and administration

Directions for adults 18 years of age and older this product is to be used once a day (every 24 hours), every day for 14 days it may take 1 to 4 days for full effect; some people get complete relief of symptoms within 24 hours       14-Day Course of Treatment swallow 1 tablet with a glass of water before eating in the morning take every day for 14 days do not take more than 1 tablet a day do not use for more than ...

Storage and handling

Other information read the directions and warnings before use keep the carton. It contains important information. store at 20-25°C (68-77°F) and protect from moisture

Label contents#

Full prescribing information#

ACTIVE INGREDIENT(S)

OTC - ACTIVE INGREDIENT SECTION

Active ingredient (in each tablet)                                         
Omeprazole, USP 20 mg 
(equivalent to 20.6 mg omeprazole magnesium)


PURPOSE

OTC - PURPOSE SECTION

Purpose 
Acid reducer



USE(S)

INDICATIONS & USAGE SECTION

Uses
• treats frequent heartburn (occurs 2 or more days a week)
• not intended for immediate relief of heartburn; this drug may take 1 to 4 days for full effect




WARNINGS

WARNINGS SECTION

Warnings
Allergy alert: 

  • Do not use if you are allergic to Omeprazole
  • Omeprazole may cause severe skin reactions. Symptoms include:
    • skin reddening
    • blisters
    • rash
    If an allergic reaction occurs, stop use and seek medical attention right away.

DO NOT USE

OTC - DO NOT USE SECTION

Do not use if you have:
• trouble or pain swallowing food, vomiting with blood, or bloody or black stools
• heartburn with lightheadedness, sweating or dizziness
• chest pain or shoulder pain with shortness of breath; sweating; pain spreading to arms, neck or shoulders; or lightheadedness
• frequent chest pain
These may be signs of a serious condition. See your doctor.



ASK A DOCTOR BEFORE USE IF

OTC - ASK DOCTOR SECTION

Ask a doctor before use if you have:
• had heartburn over 3 months. This may be a sign of a more serious condition.
• frequent wheezing, particularly with heartburn
• unexplained weight loss
• nausea or vomiting
• stomach pain



ASK A DOCTOR OR PHARMACIST BEFORE USE IF

OTC - ASK DOCTOR/PHARMACIST SECTION

Ask a doctor or pharmacist before use if you are taking a prescription drug. 
Acid reducers may interact with certain prescription drugs.



STOP USE AND ASK DOCTOR IF

OTC - STOP USE SECTION

Stop use and ask a doctor if
• your heartburn continues or worsens
• you need to take this product for more than 14 days
• you need to take more than 1 course of treatment every 4 months
• you get diarrhea
• you develop a rash or joint pain



PREGNANCY/BREASTFEEDING

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding, ask a health professional before use.

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.  In case of overdose, get medical help or contact a Poison Control Center right away (1-800-222-1222).

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

Directions

  • for adults 18 years of age and older
  • this product is to be used once a day (every 24 hours), every day for 14 days
  • it may take 1 to 4 days for full effect; some people get complete relief of symptoms within 24 hours

      14-Day Course of Treatment

  • swallow 1 tablet with a glass of water before eating in the morning
  • take every day for 14 days
  • do not take more than 1 tablet a day
  • do not use for more than 14 days unless directed by your doctor
  • swallow whole. Do not chew or crush tablets.

      Repeated 14-Day Courses (if needed)

  • you may repeat a 14-day course every 4 months
  • do not take for more than 14 days or more often than every 4 months unless directed by a doctor
  • children under 18 years of age: ask a doctor. Heartburn in children may sometimes be caused by a serious condition.

STORAGE

STORAGE AND HANDLING SECTION

Other information

  • read the directions and warnings before use
  • keep the carton. It contains important information.
  • store at 20-25°C (68-77°F) and protect from moisture

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Inactive ingredients 
colloidal silicone dioxide, crospovidone, glyceryl monostearate, hydroxypropyl cellulose, hypromellose, magnesium stearate, methacrylic acid and ethyl acrylate copolymer, microcrystalline cellulose, polyethylene glycol 400, polyethylene glycol 6000, polysorbate 80, red iron oxide, simethicone, sodium stearyl fumarate, starch, sucrose, talc, titanium dioxide, triethyl citrate



QUESTIONS OR COMMENTS

SPL UNCLASSIFIED SECTION

Questions or comments? Call 1-877-376-4271 (weekdays 9 AM to 5 PM)

Tips for Managing Heartburn 

• Do not lie flat or bend over after eating. 
• Do not wear tight-fitting clothing around the stomach.
• Do not eat before bedtime. 
• Raise the head of your bed. 
• Avoid heartburn-causing foods such as rich, spicy, fatty or fried foods, chocolate, caffeine,     alcohol and certain fruits and vegetables.      
• Eat slowly and do not eat big meals.
• If overweight, lose weight. 
• Quit smoking. 

Manufactured for:
Time-Cap Labs, Inc. 
7 Michael Avenue, 
Farmingdale, 
NY 11735, USA

Manufactured by: 
Marksans Pharma Ltd.
Plot No. L-82, L-83
Verna Indl. Estate
Verna, Goa-403722, India  



PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC: 25000-091-76
Omeprazole Delayed-Release Tablets 20 mg 
14's count Carton 


omeprazole-14s-blister-carton
omeprazole-14s-blister-carton


NDC: 25000-091-76
Omeprazole Delayed-Release Tablets 20 mg 
14's count Label 


omeprazole-14s-bottle-pack-label
omeprazole-14s-bottle-pack-label


NDC: 25000-091-77
Omeprazole Delayed-Release Tablets 20 mg 
14's count (2 x 7's blister) Carton


omeprazole-14s-blisterpack-cartonomeprazole-14s-blisterpack-carton


DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
402014omeprazole 20 MG Delayed Release Oral TabletPSN3
402014omeprazole 20 MG Delayed Release Oral TabletSCD3
402014omeprazole 20 MG (as omeprazole magnesium 20.6 MG) Delayed Release Oral TabletSY3

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
OMEPRAZOLE Pharmacologic Class Indexing3Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
dc7c5daa-021f-40dd-b00d-63982cb2067aProduct name120230426
873ef493-6b37-49d8-ac7f-bfca4117d2c1Product name520210607
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name520200925
f33561b9-47cb-411c-a228-16c62e346cd4Product name120200415
ade821ba-260a-47e2-bd89-743e27ac9906Product name120161121
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name220160823

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
25000-091-76Omeprazole 20 mg1 in 1 CARTONTABLET, DELAYED RELEASE13
25000-091-76Omeprazole 20 mg14 in 1 BOTTLETABLET, DELAYED RELEASE143
25000-091-77Omeprazole 20 mg7 in 1 BLISTER PACKTABLET, DELAYED RELEASE73
25000-091-77Omeprazole 20 mg2 in 1 CARTONTABLET, DELAYED RELEASE23

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 22 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
25000-09125000-091-77, 25000-091-76

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 20 matching rows.

Source Document#

Source XML

Orange Book application contexts#

All distinct exact application/product contexts derived from this label’s complete NDC list are paginated below.

Orange Book application contexts page 1 of 1 · 1 matching rows.

Source provenance: Browse the complete Orange Book source catalog · source snapshot 43.

Orange Book products#

Current product rows page 1 of 1 · 1 matching rows.

Application-product, Trade name, Ingredient table
Application-productTrade nameIngredientStrengthDosage form / routeTE codesRLD / RSApproval date
A218829-001OMEPRAZOLE MAGNESIUMOMEPRAZOLE MAGNESIUMEQ 20MG BASETABLET, DELAYED RELEASE / ORAL2025-08-07

Observed Orange Book product history#

Observed FDA ZIP history: Each table is queried independently by exact application/product key from successfully parsed Orange Book snapshots. Capture times identify archived source observations; absence or a change between snapshots is not inferred. FDA publication files that were not recoverable as structured ZIP data are not represented as states.

Captured, Edition, Application-product table
CapturedEditionApplication-productTrade nameStrengthDosage form / routeProduct TE source textRLD / RSApproval dateSource SHA-256
2026-09-14 22:38:342026-08A218829-001OMEPRAZOLE MAGNESIUMEQ 20MG BASETABLET, DELAYED RELEASE / ORAL2025-08-0784e616aacf4f…
2026-08-18 06:07:402026-07A218829-001OMEPRAZOLE MAGNESIUMEQ 20MG BASETABLET, DELAYED RELEASE / ORAL2025-08-07caaa826d4ba7…
2026-02-19 14:30 UTC2026-02A218829-001OMEPRAZOLE MAGNESIUMEQ 20MG BASETABLET, DELAYED RELEASE / ORAL2025-08-07011fe1cb6892…
2025-12-14 10:44 UTC · 2 captures of this ZIP2025-12A218829-001OMEPRAZOLE MAGNESIUMEQ 20MG BASETABLET, DELAYED RELEASE / ORAL2025-08-0731067a03dcf5…
2026-07-26 02:55 UTC · 3 captures of this ZIP2026-06A218829-001OMEPRAZOLE MAGNESIUMEQ 20MG BASETABLET, DELAYED RELEASE / ORAL2025-08-07a50c72e98297…

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Omeprazole 20 mgOMEPRAZOLE 20 MGMARKSANS PHARMA LIMITED921bf750-9dd7-42ff-82bb-043b03f0fe692025-08-11WarningsExact identifier
ndc (package): 25000-091-77
ndc (package): 25000-091-76
ndc (product): 25000-091
ndc11 (package): 25000009176
ndc11 (package): 25000009177
spl id: dcf79426-6aec-432a-aabe-dcb98c0f2cec
spl set id: 921bf750-9dd7-42ff-82bb-043b03f0fe69

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.