65597-302 : Morphabond 30 mg Oral Tablet, Extended Release


NDC65597-302
Labeler: Daiichi Sankyo Inc.
Product Type: Human Prescription Drug
Drug Name:  Morphabond
Dosage Form: Oral Tablet, Extended Release
Application #: NDA206544
Rev. Date: 
CSA Schedule: CII (US) [1]


[1] Schedule II / IIN Controlled Substance: High potential for abuse which may lead to severe psychological or physical dependence. (i.e. Narcotics such as Dilaudid, Methadone, Demerol, Oxycodone, Percocet, Fentanyl, Morphine, Opium, Codeine, and Hydrocodone ... Schedule IIN stimulants include non-narcotic Amphetamines such as Dexedrine, Adderall, Desoxyn, Methylphenidate (Ritalin) ... Other Schedule II substances include Amobarbital, Glutethimide, and Pentobarbital. More Details: US Dept of Justice Controlled Substance Schedules.

Appearance:


Markings: IDT;M30
Shapes:  Round
Colors:  Purple
Size (mm): 11
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:

  • 65597-302-10: 100 TABLET, EXTENDED RELEASE IN 1 BOTTLE, PLASTIC (65597‑302‑10)

Active Ingredients:

  • Morphine Sulfate

Dosage Strength:

  • 30 mg

Pharmaceutical Classes:

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

Related Products:

Based on records with the same trade name.
  • 65597-301 Morphabond 15 mg Oral Tablet, Extended Release by Daiichi Sankyo Inc.
  • 65597-303 Morphabond 60 mg Oral Tablet, Extended Release by Daiichi Sankyo Inc.
  • 65597-304 Morphabond 100 mg Oral Tablet, Extended Release by Daiichi Sankyo Inc.
  • 69296-001 Morphabond 100 mg Oral Tablet, Extended Release by Inspirion Delivery Technologies, LLC
  • 69296-002 Morphabond 60 mg Oral Tablet, Extended Release by Inspirion Delivery Technologies, LLC
  • 69296-003 Morphabond 30 mg Oral Tablet, Extended Release by Inspirion Delivery Technologies, LLC
  • 69296-004 Morphabond 15 mg Oral Tablet, Extended Release by Inspirion Delivery Technologies, LLC

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.