10191-1001 : Morphinum 3 [hp_x]/1 Sublingual Pellet


NDC10191-1001
Labeler: Remedy Makers
Product Type: Human Prescription Drug
Drug Name: Morphinum
Dosage Form: Sublingual Pellet
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.

NDC Package Codes:

  • 10191-1001-2: 162 PELLET IN 1 VIAL, GLASS (10191‑1001‑2)

Active Ingredients:

  • Abt-925 Anhydrous Free Base

Dosage Strength:

  • 3 [hp_X]/1

Related Products:

Based on records with the same trade name.
  • 10191-1002 Morphinum 6 [hp_x]/1 Sublingual Pellet by Remedy Makers
  • 10191-1003 Morphinum 9 [hp_x]/1 Sublingual Pellet by Remedy Makers
  • 10191-1004 Morphinum 12 [hp_x]/1 Sublingual Pellet by Remedy Makers
  • 10191-1005 Morphinum 15 [hp_x]/1 Sublingual Pellet by Remedy Makers
  • 10191-1013 Morphinum 30 [hp_c]/1 Sublingual Pellet by Remedy Makers

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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.