49884-663 : Candesartan Cilexetil 32 mg / Hctz 12.5 mg Oral Tablet


NDC: 49884-663
Labeler: Par Pharmaceutical Inc.
Product Type: Human Prescription Drug
Drug Name:  Candesartan Cilexetil-hydrochlorothiazide
Dosage Form: Oral Tablet
Application #: NDA021093
Rev. Date: 


Appearance:


Markings: ACJ
Shapes:  Oval
Colors:  Yellow
Size (mm): 11
Segments: * 2

* Segments = the number of equally sized pieces which the pill can be broken into. In this case, a value of 2 indicates a scored pill which can be broken into 2 equal pieces.

NDC Package Codes:

  • 49884-663-09: 90 TABLET IN 1 BOTTLE (49884‑663‑09)

Active Ingredients:

  • Candesartan Cilexetil
  • Hydrochlorothiazide

Dosage Strength:

  • 32 mg
  • 12.5 mg

Inactive Ingredients:

  • Carboxymethylcellulose Calcium
  • Hydroxypropyl Cellulose (Type H)
  • Lactose Monohydrate
  • Magnesium Stearate
  • Starch, Corn
  • Polyethylene Glycol 8000
  • Ferric Oxide Yellow

Pharmaceutical Classes:

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

Related Products:

Based on records with the same trade name.
  • 49884-662 Candesartan Cilexetil 16 mg / Hctz 12.5 mg Oral Tablet by Par Pharmaceutical Inc.
  • 49884-664 Candesartan Cilexetil 32 mg / Hctz 25 mg Oral Tablet by Par Pharmaceutical Inc.

NDC QR Code

Scan the QR code below to easily reference this data in the future:

NDC 49884-663 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.