0121-2036 : Buprenorphine and Naloxone Sublingual Tablet


NDC0121-2036
Labeler: Pai Holdings, LLC Dba Pharmaceutical Associates, Inc. and Dba Pai Pharma
Product Type: Human Prescription Drug
Drug Name:  Buprenorphine and Naloxone
Dosage Form: Sublingual Tablet
Application #: ANDA204431
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:

  • 0121-2036-30: 30 TABLET IN 1 BOTTLE, PLASTIC (0121‑2036‑30)

Active Ingredients:

  • Buprenorphine Hydrochloride
  • Naloxone Hydrochloride

Dosage Strength:

  • 8 mg
  • 2 mg

Pharmaceutical Classes:

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

Related Products:

Based on records with the same trade name.
  • 0121-1018 Buprenorphine and Naloxone Sublingual Tablet by Pai Holdings, LLC Dba Pharmaceutical Associates, Inc. and Dba Pai Pharma
  • 0093-5720 Buprenorphine and Naloxone Sublingual Tablet by Teva Pharmaceuticals USA Inc
  • 0093-5721 Buprenorphine and Naloxone Sublingual Tablet by Teva Pharmaceuticals USA Inc
  • 0378-8765 Buprenorphine and Naloxone Buccal; Sublingual Film by Mylan Pharmaceuticals Inc.
  • 0378-8766 Buprenorphine and Naloxone Buccal; Sublingual Film by Mylan Pharmaceuticals Inc.
  • 0378-8767 Buprenorphine and Naloxone Buccal; Sublingual Film by Mylan Pharmaceuticals Inc.
  • 0378-8768 Buprenorphine and Naloxone Buccal; Sublingual Film by Mylan Pharmaceuticals Inc.
  • 0781-7216 Buprenorphine and Naloxone Buccal; Sublingual Film, Soluble by Sandoz Inc
  • 0781-7227 Buprenorphine and Naloxone Buccal; Sublingual Film, Soluble by Sandoz Inc
  • 0781-7238 Buprenorphine and Naloxone Buccal; Sublingual Film, Soluble by Sandoz Inc
  • 0781-7249 Buprenorphine and Naloxone Buccal; Sublingual Film, Soluble by Sandoz Inc
  • 24555-0970 Buprenorphine and Naloxone Sublingual Tablet by Correct Rx Pharmacy Services, Inc.
  • 42858-601 Buprenorphine and Naloxone Sublingual Tablet by Rhodes Parmaceuticals L.p.
  • 42858-602 Buprenorphine and Naloxone Sublingual Tablet by Rhodes Parmaceuticals L.p.
  • 43598-579 Buprenorphine and Naloxone Buccal; Sublingual Film, Soluble by Dr.reddys Laboratories Inc
  • 43598-580 Buprenorphine and Naloxone Buccal; Sublingual Film, Soluble by Dr.reddys Laboratories Inc
  • 43598-581 Buprenorphine and Naloxone Buccal; Sublingual Film, Soluble by Dr.reddys Laboratories Inc
  • 43598-582 Buprenorphine and Naloxone Buccal; Sublingual Film, Soluble by Dr.reddys Laboratories Inc
  • 50383-287 Buprenorphine and Naloxone Sublingual Tablet by Hi-tech Pharmacal Co., Inc.
  • 50383-294 Buprenorphine and Naloxone Sublingual Tablet by Hi-tech Pharmacal Co., Inc.
  • 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.