10202-722 : Acid Reducer 20 mg Oral Tablet, Delayed Release


NDC: 10202-722
Labeler: 7-eleven
Product Type: Human OTC Drug
Drug Name: Acid Reducer
Dosage Form: Oral Tablet, Delayed Release
Application #: ANDA206877
Rev. Date: 


Appearance:


Markings: Z;69
Shapes:  Rectangle (4 sides)
Colors:  Pink
Size (mm): 14
Segments: * 1

* Segments = the number of equally sized pieces which the pill can be broken into. In this case, a value of 1 indicates a solid pill with no score lines.

NDC Package Codes:

  • 10202-722-05: 1 BOTTLE IN 1 CARTON (10202‑722‑05) > 14 TABLET, DELAYED RELEASE IN 1 BOTTLE

Active Ingredients:

  • Omeprazole Magnesium

Dosage Strength:

  • 20 mg

Inactive Ingredients:

  • Crospovidone (12 Mpa.s At 5%)
  • Glyceryl Monostearate
  • Hydroxypropyl Cellulose (90000 Wamw)
  • Hypromellose 2910 (5 Mpa.s)
  • Magnesium Stearate
  • Methacrylic Acid - Ethyl Acrylate Copolymer (1:1) Type a
  • Microcrystalline Cellulose
  • Polyethylene Glycol 4000
  • Polysorbate 80
  • Ferric Oxide Red
  • Silicon Dioxide
  • Sodium Hydroxide
  • Sodium Stearyl Fumarate
  • Dextrose, Unspecified Form
  • Starch, Corn
  • Sucrose
  • Talc
  • Titanium Dioxide
  • Triethyl Citrate
  • Ferric Oxide Yellow
  • Hydroxypropyl Cellulose (45000 Wamw)
  • Hypromellose 2910 (6 Mpa.s) /

Pharmaceutical Classes:

  • Cytochrome P450 2C19 Inhibitors [MoA]
  • Proton Pump Inhibitor [EPC]
  • Proton Pump Inhibitors [MoA]

Related Products:

Based on records with the same trade name.
  • 0113-0047 Ranitidine 150 mg (As Ranitidine Hydrochloride 168 mg) Oral Tablet by L. Perrigo Company
  • 0113-2141 Acid Reducer 10 mg Oral Tablet by L. Perrigo Company
  • 0363-1008 Acid Reducer 20 mg Oral Tablet, Delayed Release by Walgreen Co.
  • 0363-9977 Acid Reducer 20 mg Oral Tablet by Walgreens
  • 0536-1322 Acid Reducer 20 mg Oral Tablet, Delayed Release by Rugby Laboratories
  • 11822-0022 Cimetidine 200 mg Oral Tablet by Rite Aid Corporation
  • 11822-0047 Ranitidine 150 mg (As Ranitidine Hydrochloride 168 mg) Oral Tablet by Rite Aid Corporation
  • 11822-0141 Famotidine 10 mg Oral Tablet by Rite Aid Corporation
  • 11822-0194 Famotidine 20 mg Oral Tablet by Rite Aid Corporation
  • 11822-0271 Ranitidine 75 mg (As Ranitidine Hydrochloride 84 mg) Oral Tablet by Rite Aid Corporation
  • 11822-0852 Acid Reducer (Ranitidine 150 mg) by Rite Aid Corporation
  • 11822-5600 Acid Reducer 20 mg Oral Capsule, Delayed Release by Rite Aid Corporation
  • 21130-003 Acid Reducer 75 mg/1 Oral Tablet, Film Coated by Safeway Inc.
  • 21130-047 Ranitidine 150 mg (As Ranitidine Hydrochloride 168 mg) Oral Tablet by Safeway
  • 21130-271 Ranitidine 75 mg (As Ranitidine Hydrochloride 84 mg) Oral Tablet by Safeway
  • 30142-077 Acid Reducer 20 mg Oral Tablet, Delayed Release by Kroger Company
  • 30142-323 Acid Reducer 200 mg Oral Tablet by Kroger Company
  • 37012-047 Ranitidine 150 mg (As Ranitidine Hydrochloride 168 mg) Oral Tablet by Shopko Stores Operating Co., LLC
  • 37012-271 Ranitidine 75 mg (As Ranitidine Hydrochloride 84 mg) Oral Tablet by Shopko Stores Operating Co., LLC
  • 37012-852 Acid Reducer 150 mg/1 Oral Tablet, Film Coated by Shopko Stores Operating Co., LLC
  • More related products ...

NDC QR Code

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NDC 10202-722 QR Code

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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.