0615-7667 : Nabumetone 750 mg Oral Tablet


NDC0615-7667
Labeler: Ncs Healthcare of Ky, Inc Dba Vangard Labs
Product Type: Human Prescription Drug
Drug Name:  Nabumetone
Dosage Form: Oral Tablet, Film Coated
Application #: ANDA075189
Rev. Date: 


Appearance:


Markings: 93;16
Shapes:  Oval
Colors:  Brown
Size (mm): 20
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.

93 16: (0093-1016) Nabumetone 750 mg Oral Tablet by Ncs Healthcare of Ky, Inc Dba Vangard Labs
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:

  • 0615-7667-39: 30 TABLET, FILM COATED IN 1 BLISTER PACK (0615‑7667‑39)

Active Ingredients:

  • Nabumetone

Dosage Strength:

  • 750 mg

Inactive Ingredients:

  • Silicon Dioxide
  • Hypromelloses
  • Cellulose, Microcrystalline
  • Polyethylene Glycols
  • Sodium Lauryl Sulfate
  • Sodium Starch Glycolate Type a Potato
  • Talc
  • Titanium Dioxide
  • Ferrosoferric Oxide
  • Ferric Oxide Red
  • Ferric Oxide Yellow

Pharmaceutical Classes:

  • Cyclooxygenase Inhibitors [MoA]
  • Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient]
  • Nonsteroidal Anti-inflammatory Drug [EPC]

Related Products:

Based on records with the same trade name.
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  • 0615-7645 Nabumetone 500 mg Oral Tablet by Ncs Healthcare of Ky, Inc Dba Vangard Labs
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NDC QR Code

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