0093-3603 : Buprenorphine 20 ug/H Transdermal Patch, Extended Release


NDC: 0093-3603
Labeler: Teva Pharmaceuticals USA, Inc.
Product Type: Human Prescription Drug
Drug Name:  Buprenorphine
Dosage Form: Transdermal Patch, Extended Release
Application #: NDA021306
Rev. Date: 
CSA Schedule: CIII (US) [1]


[1] Schedule III / IIIN Controlled Substance: Has a potential for abuse less than substances in Schedules I or II and abuse may lead to moderate or low physical dependence or high psychological dependence. (i.e. Products containing not more than 90 milligrams of Codeine per dosage unit [such as Tylenol with Codeine], other narcotics such as Buprenorphine (Suboxone), and Schedule IIIN non-narcotics such as Didrex, Ketamine, Phendimetrazine, and Anabolic Steroids). More Details: US Dept of Justice Controlled Substance Schedules.

NDC Package Codes:

  • 0093-3603-40: 4 POUCH IN 1 CARTON (0093‑3603‑40) > 1 PATCH IN 1 POUCH (0093‑3603‑21) > 168 H IN 1 PATCH

Active Ingredients:

  • Buprenorphine

Dosage Strength:

  • 20 ug/h

Pharmaceutical Classes:

  • Partial Opioid Agonists [MoA]
  • Partial Opioid Agonist [EPC]

Related Products:

Based on records with the same trade name.
  • 0093-3239 Buprenorphine 7.5 ug/H Transdermal Patch, Extended Release by Teva Pharmaceuticals USA, Inc.
  • 0093-3600 Buprenorphine 5 ug/H Transdermal Patch, Extended Release by Teva Pharmaceuticals USA, Inc.
  • 0093-3601 Buprenorphine 10 ug/H Transdermal Patch, Extended Release by Teva Pharmaceuticals USA, Inc.
  • 0093-3602 Buprenorphine 15 ug/H Transdermal Patch, Extended Release by Teva Pharmaceuticals USA, Inc.
  • 0093-3656 Buprenorphine 5 ug/H Transdermal Patch, Extended Release by Teva Pharmaceuticals USA, Inc.
  • 0093-3657 Buprenorphine 10 ug/H Transdermal Patch, Extended Release by Teva Pharmaceuticals USA, Inc.
  • 0093-3658 Buprenorphine 15 ug/H Transdermal Patch, Extended Release by Teva Pharmaceuticals USA, Inc.
  • 0093-3659 Buprenorphine 20 ug/H Transdermal Patch, Extended Release by Teva Pharmaceuticals USA, Inc.
  • 0228-3153 Buprenorphine 8 mg Sublingual Tablet by Actavis Pharma, Inc.
  • 0228-3156 Buprenorphine 2 mg Sublingual Tablet by Actavis Pharma, Inc.
  • 24555-0002 Buprenorphine 2 mg Sublingual Tablet by Correct Rx Pharmacy Services, Inc.
  • 24555-0008 Buprenorphine 8 mg Sublingual Tablet by Correct Rx Pharmacy Services, Inc.
  • 24555-2222 Buprenorphine 2 mg Sublingual Tablet by Correct Rx Pharmacy Services, Inc.
  • 24555-8888 Buprenorphine 8 mg Sublingual Tablet by Correct Rx Pharmacy Services, Inc.
  • 42858-353 Buprenorphine 7.5 ug/H Transdermal Patch by Rhodes Pharmaceuticals L.p.
  • 42858-493 Buprenorphine 10 ug/H Transdermal Patch by Rhodes Pharmaceuticals L.p.
  • 42858-501 Buprenorphine 2 mg Sublingual Tablet by Rhodes Pharmaceuticals L.p.
  • 42858-502 Buprenorphine 8 mg Sublingual Tablet by Rhodes Pharmaceuticals L.p.
  • 42858-586 Buprenorphine 15 ug/H Transdermal Patch by Rhodes Pharmaceuticals L.p.
  • 42858-750 Buprenorphine 5 ug/H Transdermal Patch by Rhodes Pharmaceuticals L.p.
  • More related products ...

NDC 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.