70518-2737 : Losartan Potassium and Hydrochlorothiazide Oral Tablet, Film Coated


NDC: 70518-2737
Labeler: Remedyrepack Inc.
Product Type: Human Prescription Drug
Drug Name:  Losartan Potassium and Hydrochlorothiazide
Dosage Form: Oral Tablet, Film Coated
Application #: ANDA091629
Rev. Date: 


Appearance:


Markings: E;49
Shapes:  Oval
Colors:  Yellow
Size (mm): 17
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.

E 49: (16714-225) Losartan Potassium and Hydrochlorothiazide Oral Tablet, Film Coated by Remedyrepack Inc.
The above image is provided by the U.S. National Library of Medicine (NLM) and is not part of the official label.

NDC Package Codes:

  • 70518-2737-0: 30 TABLET, FILM COATED IN 1 BOTTLE, PLASTIC (70518‑2737‑0)
  • 70518-2737-1: 90 TABLET, FILM COATED IN 1 BOTTLE, PLASTIC (70518‑2737‑1)
  • 70518-2737-2: 30 TABLET, FILM COATED IN 1 BLISTER PACK (70518‑2737‑2)

Active Ingredients:

  • Hydrochlorothiazide
  • Losartan Potassium

Dosage Strength:

  • 25 mg
  • 100 mg

Inactive Ingredients:

  • Silicon Dioxide
  • Hydroxypropyl Cellulose (1600000 Wamw)
  • Hypromellose 2910 (6 Mpa.s)
  • Lactose Monohydrate
  • Magnesium Stearate
  • Microcrystalline Cellulose
  • Starch, Corn
  • Titanium Dioxide
  • D&c Yellow No. 10 /

Pharmaceutical Classes:

  • Angiotensin 2 Receptor Antagonists [MoA]
  • Angiotensin 2 Receptor Blocker [EPC]
  • Increased Diuresis [PE]
  • Thiazide Diuretic [EPC]
  • Thiazides [CS]

Related Products:

Based on records with the same trade name.
  • 70518-0112 Losartan Potassium and Hydrochlorothiazide Oral Tablet by Remedyrepack Inc.
  • 70518-0354 Losartan Potassium and Hydrochlorothiazide Oral Tablet by Remedyrepack Inc.
  • 70518-0602 Losartan Potassium and Hydrochlorothiazide Oral Tablet, Film Coated by Remedyrepack Inc.
  • 70518-0786 Losartan Potassium and Hydrochlorothiazide Oral Tablet, Film Coated by Remedyrepack Inc.
  • 70518-1526 Losartan Potassium and Hydrochlorothiazide Oral Tablet by Remedyrepack Inc.
  • 70518-1682 Losartan Potassium and Hydrochlorothiazide Oral Tablet, Film Coated by Remedyrepack Inc.
  • 70518-1943 Losartan Potassium and Hydrochlorothiazide Oral Tablet, Film Coated by Remedyrepack Inc.
  • 70518-2057 Losartan Potassium and Hydrochlorothiazide Oral Tablet, Film Coated by Remedyrepack Inc.
  • 70518-2417 Losartan Potassium and Hydrochlorothiazide Oral Tablet, Film Coated by Remedyrepack Inc.
  • 70518-2564 Losartan Potassium and Hydrochlorothiazide Oral Tablet by Remedyrepack Inc.
  • 70518-2578 Losartan Potassium and Hydrochlorothiazide Oral Tablet by Remedyrepack Inc.
  • 70518-3231 Losartan Potassium and Hydrochlorothiazide Oral Tablet, Film Coated by Remedyrepack Inc.
  • 70518-3398 Losartan Potassium and Hydrochlorothiazide Oral Tablet, Film Coated by Remedyrepack Inc.
  • 70518-3404 Losartan Potassium and Hydrochlorothiazide Oral Tablet, Film Coated by Remedyrepack Inc.
  • 70518-3409 Losartan Potassium and Hydrochlorothiazide Oral Tablet, Film Coated by Remedyrepack Inc.
  • 70518-3420 Losartan Potassium and Hydrochlorothiazide Oral Tablet, Film Coated by Remedyrepack Inc.
  • 52125-397 Hctz 12.5 mg Oral Tablet by Remedyrepack Inc.
  • 52125-399 Hctz 25 mg / Losartan Potassium 100 mg Oral Tablet by Remedyrepack Inc.
  • 52125-452 Hctz 12.5 mg / Losartan Potassium 100 mg Oral Tablet by Remedyrepack Inc.
  • 52125-473 Hctz 12.5 mg / Losartan Potassium 50 mg Oral Tablet by Remedyrepack Inc.
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NDC QR Code

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NDC 70518-2737 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.