0115-5311 : Bendroflumethiazide 5 mg / Nadolol 40 mg Oral Tablet


NDC: 0115-5311
Labeler: Global Pharmaceuticals, Division of Impax Laboratories, Inc.
Product Type: Human Prescription Drug
Drug Name:  Nadolol and Bendroflumethiazide
Dosage Form: Oral Tablet
Application #: ANDA077833
Rev. Date: 


Appearance:


Markings: G;531
Shapes:  Round
Colors:  White
Size (mm): 9
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:

  • 0115-5311-01: 100 TABLET IN 1 BOTTLE (0115‑5311‑01)
  • 0115-5311-02: 500 TABLET IN 1 BOTTLE (0115‑5311‑02)

Active Ingredients:

  • Bendroflumethiazide
  • Nadolol

Dosage Strength:

  • 5 mg
  • 40 mg

Inactive Ingredients:

  • Croscarmellose Sodium
  • Hypromelloses
  • Lactose Monohydrate
  • Magnesium Stearate
  • Mannitol
  • Cellulose, Microcrystalline
  • Starch, Corn
  • Talc

Pharmaceutical Classes:

  • Adrenergic beta-Antagonists [MoA]
  • beta-Adrenergic Blocker [EPC]
  • Increased Diuresis [PE]
  • Thiazide Diuretic [EPC]
  • Thiazides [Chemical/Ingredient]

Related Products:

Based on records with the same trade name.
  • 0115-5322 Bendroflumethiazide 5 mg / Nadolol 80 mg Oral Tablet by Global Pharmaceuticals, Division of Impax Laboratories, Inc.

NDC QR Code

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

NDC 0115-5311 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.