47335-617 : Duloxetine 30 mg Oral Capsule, Delayed Release


NDC: 47335-617
Labeler: Sun Pharmaceutical Industries, Inc.
Product Type: Human Prescription Drug
Drug Name:  Duloxetine
Dosage Form: Oral Capsule, Delayed Release
Application #: NDA212516
Rev. Date: 


Appearance:


Markings: RG;54
Shapes:  Capsule
Colors:  White / Blue
Size (mm): 16
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:

  • 47335-617-10: 1000 CAPSULE, DELAYED RELEASE IN 1 BOTTLE (47335‑617‑10)
  • 47335-617-30: 30 CAPSULE, DELAYED RELEASE IN 1 BOTTLE (47335‑617‑30)
  • 47335-617-60: 60 CAPSULE, DELAYED RELEASE IN 1 BOTTLE (47335‑617‑60)
  • 47335-617-90: 90 CAPSULE, DELAYED RELEASE IN 1 BOTTLE (47335‑617‑90)

Active Ingredients:

  • Duloxetine Hydrochloride

Dosage Strength:

  • 30 mg

Inactive Ingredients:

  • Talc
  • Titanium Dioxide
  • D&c Yellow No. 10
  • Fd&c Blue No. 1
  • Fd&c Red No. 40
  • Gelatin, Unspecified
  • Sodium Lauryl Sulfate
  • Ferrosoferric Oxide
  • Shellac
  • Ammonia
  • Fd&c Red No. 3
  • Hypromellose, Unspecified
  • Hypromellose Phthalate (24% Phthalate, 55 Cst)
  • Polyethylene Glycol, Unspecified
  • Sucrose
  • Starch, Corn
  • Triethyl Citrate
  • Propylene Glycol /

Pharmaceutical Classes:

  • Norepinephrine Uptake Inhibitors [MoA]
  • Serotonin and Norepinephrine Reuptake Inhibitor [EPC]
  • Serotonin Uptake Inhibitors [MoA]

Related Products:

Based on records with the same trade name.
  • 47335-616 Duloxetine 20 mg Oral Capsule, Delayed Release by Sun Pharmaceutical Industries, Inc.
  • 47335-618 Duloxetine 40 mg Oral Capsule, Delayed Release by Sun Pharmaceutical Industries, Inc.
  • 47335-619 Duloxetine 60 mg Oral Capsule, Delayed Release by Sun Pharmaceutical Industries, Inc.
  • 47335-381 Duloxetine 20 mg/1 Oral Capsule, Delayed Release by Sun Pharma Global Fze
  • 47335-382 Duloxetine 30 mg/1 Oral Capsule, Delayed Release by Sun Pharma Global Fze
  • 47335-383 Duloxetine 60 mg/1 Oral Capsule, Delayed Release by Sun Pharma Global Fze
  • 0093-7542 Duloxetine 20 mg/1 Oral Capsule, Delayed Release by Teva Pharmaceuticals USA Inc
  • 0093-7543 Duloxetine 30 mg/1 Oral Capsule, Delayed Release by Teva Pharmaceuticals USA Inc
  • 0093-7544 Duloxetine 60 mg/1 Oral Capsule, Delayed Release by Teva Pharmaceuticals USA Inc
  • 0179-0144 Duloxetine 20 mg/1 Oral Capsule, Delayed Release by Kaiser Foundation Hospitals
  • 0228-2890 Duloxetine 20 mg/1 Oral Capsule, Delayed Release by Actavis Elizabeth LLC
  • 0228-2891 Duloxetine 30 mg/1 Oral Capsule, Delayed Release by Actavis Elizabeth LLC
  • 0228-2892 Duloxetine 60 mg/1 Oral Capsule, Delayed Release by Actavis Elizabeth LLC
  • 0615-8494 Duloxetine 20 mg Oral Capsule, Delayed Release by Ncs Healthcare of Ky, LLC Dba Vangard Labs
  • 0615-8495 Duloxetine 30 mg Oral Capsule, Delayed Release by Ncs Healthcare of Ky, LLC Dba Vangard Labs
  • 0615-8496 Duloxetine 60 mg Oral Capsule, Delayed Release by Ncs Healthcare of Ky, LLC Dba Vangard Labs
  • 0904-7043 Duloxetine 20 mg Oral Capsule, Delayed Release by Major Pharmaceuticals
  • 0904-7044 Duloxetine 30 mg Oral Capsule, Delayed Release by Major Pharmaceuticals
  • 0904-7045 Duloxetine 60 mg Oral Capsule, Delayed Release by Major Pharmaceuticals
  • 13811-662 Duloxetine 20 mg Oral Capsule, Delayed Release by Trigen Laboratories, LLC
  • More related products ...

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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.