49884-175 : Amlodipine, Valsartan, Hydrochlorothiazide Oral Tablet, Film Coated


NDC: 49884-175
Labeler: Par Pharmaceutical Inc.
Product Type: Human Prescription Drug
Drug Name: Amlodipine, Valsartan, Hydrochlorothiazide
Dosage Form: Oral Tablet, Film Coated
Application #: ANDA201087
Rev. Date: 


Appearance:


Markings: P;175
Shapes:  Oval
Colors:  White
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:

  • 49884-175-05: 500 TABLET, FILM COATED IN 1 BOTTLE (49884‑175‑05)
  • 49884-175-09: 90 TABLET, FILM COATED IN 1 BOTTLE (49884‑175‑09)
  • 49884-175-11: 30 TABLET, FILM COATED IN 1 BOTTLE (49884‑175‑11)

Active Ingredients:

  • Amlodipine Besylate
  • Hydrochlorothiazide
  • Valsartan

Dosage Strength:

  • 10 mg
  • 25 mg
  • 320 mg

Inactive Ingredients:

  • Cellulose, Microcrystalline
  • Crospovidone
  • Fd&c Yellow No. 5
  • Ferric Oxide Red
  • Lactose Monohydrate
  • Magnesium Stearate
  • Polyethylene Glycols
  • Polyvinyl Alcohol
  • Titanium Dioxide
  • Triethyl Citrate

Pharmaceutical Classes:

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

Related Products:

Based on records with the same trade name.
  • 49884-172 Amlodipine, Valsartan, Hydrochlorothiazide Oral Tablet, Film Coated by Par Pharmaceutical Inc.
  • 49884-173 Amlodipine, Valsartan, Hydrochlorothiazide Oral Tablet, Film Coated by Par Pharmaceutical Inc.
  • 49884-174 Amlodipine, Valsartan, Hydrochlorothiazide Oral Tablet, Film Coated by Par Pharmaceutical Inc.
  • 49884-185 Amlodipine, Valsartan, Hydrochlorothiazide Oral Tablet, Film Coated by Par Pharmaceutical Inc.
  • 0781-5756 Amlodipine, Valsartan, Hydrochlorothiazide Oral Tablet, Film Coated by Sandoz Inc
  • 0781-5760 Amlodipine, Valsartan, Hydrochlorothiazide Oral Tablet, Film Coated by Sandoz Inc
  • 0781-5771 Amlodipine, Valsartan, Hydrochlorothiazide Oral Tablet, Film Coated by Sandoz Inc
  • 0781-5787 Amlodipine, Valsartan, Hydrochlorothiazide Oral Tablet, Film Coated by Sandoz Inc
  • 0781-5794 Amlodipine, Valsartan, Hydrochlorothiazide Oral Tablet, Film Coated by Sandoz Inc
  • 51407-668 Amlodipine, Valsartan, Hydrochlorothiazide Oral Tablet, Film Coated by Golden State Medical Supply, Inc.
  • 51407-669 Amlodipine, Valsartan, Hydrochlorothiazide Oral Tablet, Film Coated by Golden State Medical Supply, Inc.
  • 51407-670 Amlodipine, Valsartan, Hydrochlorothiazide Oral Tablet, Film Coated by Golden State Medical Supply, Inc.
  • 51407-671 Amlodipine, Valsartan, Hydrochlorothiazide Oral Tablet, Film Coated by Golden State Medical Supply, Inc.
  • 51407-672 Amlodipine, Valsartan, Hydrochlorothiazide Oral Tablet, Film Coated by Golden State Medical Supply, Inc.
  • 64380-197 Amlodipine, Valsartan, Hydrochlorothiazide Oral Tablet, Film Coated by Strides Pharma Science Limited
  • 64380-198 Amlodipine, Valsartan, Hydrochlorothiazide Oral Tablet, Film Coated by Strides Pharma Science Limited
  • 64380-199 Amlodipine, Valsartan, Hydrochlorothiazide Oral Tablet, Film Coated by Strides Pharma Science Limited
  • 64380-200 Amlodipine, Valsartan, Hydrochlorothiazide Oral Tablet, Film Coated by Strides Pharma Science Limited
  • 64380-201 Amlodipine, Valsartan, Hydrochlorothiazide Oral Tablet, Film Coated by Strides Pharma Science Limited

NDC QR Code

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NDC 49884-175 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.