11673-753 : Up and Up Esomeprazole Magnesium 20 mg Oral Capsule, Delayed Release


NDC11673-753
Labeler: Target Corporation
Product Type: Human OTC Drug
Drug Name: Up and Up Esomeprazole Magnesium
Dosage Form: Oral Capsule, Delayed Release
Application #: ANDA207193
Rev. Date: 


Appearance:


Markings: 7U4
Shapes:  Capsule
Colors:  Blue
Size (mm): 11
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:

  • 11673-753-01: 1 BOTTLE IN 1 CARTON (11673‑753‑01) > 14 CAPSULE, DELAYED RELEASE IN 1 BOTTLE
  • 11673-753-03: 3 BOTTLE IN 1 CARTON (11673‑753‑03) > 14 CAPSULE, DELAYED RELEASE IN 1 BOTTLE

Active Ingredients:

  • Esomeprazole Magnesium Dihydrate

Dosage Strength:

  • 20 mg

Inactive Ingredients:

  • Fd&c Blue No. 1
  • Fd&c Red No. 3
  • Ferrosoferric Oxide
  • Gelatin, Unspecified
  • Glyceryl Monostearate
  • Hypromellose, Unspecified
  • Magnesium Stearate
  • Meglumine
  • Methacrylic Acid - Ethyl Acrylate Copolymer (1:1) Type a
  • Polyethylene Glycol, Unspecified
  • Polysorbate 80
  • Shellac
  • Sodium Lauryl Sulfate
  • Talc
  • Titanium Dioxide
  • Triethyl Citrate /

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.
  • 11673-898 Up and Up Esomeprazole Magnesium 20 mg Oral Capsule, Delayed Release by Target Corporation

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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.