68382-385 : Duloxetine 20 mg Oral Capsule, Delayed Release


NDC68382-385
Labeler: Zydus Pharmaceuticals (Usa) Inc.
Product Type: Human Prescription Drug
Drug Name:  Duloxetine
Dosage Form: Oral Capsule, Delayed Release
Application #: ANDA090739
Rev. Date: 


Appearance:


Markings: 241;20;mg
Shapes:  Capsule
Colors:  Green / White
Size (mm): 14
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:

  • 68382-385-06: 30 CAPSULE, DELAYED RELEASE IN 1 BOTTLE (68382‑385‑06)
  • 68382-385-14: 60 CAPSULE, DELAYED RELEASE IN 1 BOTTLE (68382‑385‑14)
  • 68382-385-16: 90 CAPSULE, DELAYED RELEASE IN 1 BOTTLE (68382‑385‑16)

Active Ingredients:

  • Duloxetine Hydrochloride

Dosage Strength:

  • 20 mg

Inactive Ingredients:

  • Alcohol
  • Ammonia
  • Butyl Alcohol
  • D&c Yellow No. 10
  • Fd&c Blue No. 1
  • Fd&c Yellow No. 6
  • Ferric Oxide Yellow
  • Gelatin
  • Hypromellose Phthalate (31% Phthalate, 40 Cst)
  • Hypromelloses
  • Isopropyl Alcohol
  • Propylene Glycol
  • Shellac
  • Sodium Lauryl Sulfate
  • Starch, Corn
  • Sucrose
  • Talc
  • Titanium Dioxide
  • Triethyl Citrate

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.
  • 68382-241 Duloxetine 20 mg/1 Oral Capsule, Delayed Release by Zydus Pharmaceuticals (Usa) Inc.
  • 68382-242 Duloxetine 30 mg/1 Oral Capsule, Delayed Release by Zydus Pharmaceuticals (Usa) Inc.
  • 68382-243 Duloxetine 60 mg/1 Oral Capsule, Delayed Release by Zydus Pharmaceuticals (Usa) Inc.
  • 68382-386 Duloxetine 30 mg Oral Capsule, Delayed Release by Zydus Pharmaceuticals (Usa) Inc.
  • 68382-387 Duloxetine 60 mg Oral Capsule, Delayed Release by Zydus Pharmaceuticals (Usa) Inc.
  • 70710-1537 Duloxetine 20 mg Oral Capsule, Delayed Release by Zydus Pharmaceuticals (Usa) Inc.
  • 70710-1538 Duloxetine 30 mg Oral Capsule, Delayed Release by Zydus Pharmaceuticals (Usa) Inc.
  • 70710-1539 Duloxetine 60 mg Oral Capsule, Delayed Release by Zydus Pharmaceuticals (Usa) Inc.
  • 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
  • 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.