10191-1035 : Codeinum 9 [hp_x]/1 Sublingual Pellet


NDC: 10191-1035
Labeler: Remedy Makers
Product Type: Human Prescription Drug
Drug Name:  Codeinum
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:

  • 10191-1035-2: 170 PELLET IN 1 VIAL, GLASS (10191‑1035‑2)

Active Ingredients:

  • Codeine Anhydrous

Dosage Strength:

  • 9 [hp_X]/1

Pharmaceutical Classes:

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

Related Products:

Based on records with the same trade name.
  • 10191-1033 Codeinum 3 [hp_x]/1 Sublingual Pellet by Remedy Makers
  • 10191-1034 Codeinum 6 [hp_x]/1 Sublingual Pellet by Remedy Makers
  • 10191-1036 Codeinum 12 [hp_x]/1 Sublingual Pellet by Remedy Makers
  • 10191-1037 Codeinum 15 [hp_x]/1 Sublingual Pellet by Remedy Makers
  • 10191-1038 Codeinum 30 [hp_x]/1 Sublingual Pellet by Remedy Makers
  • 10191-1045 Codeinum 100 [hp_c]/1 Sublingual Pellet by Remedy Makers

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.