20482-335 : Syndros 5 mg/ml Oral Solution
| NDC: | 20482-335 |
| Labeler: | Insys Therapeutics, Inc. |
| Product Type: | Human Prescription Drug |
| Drug Name: | Syndros |
| Dosage Form: | Oral Solution |
| Application #: | NDA205525 |
| 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:
- 20482-335-30: 1 BOTTLE, GLASS IN 1 CARTON (20482‑335‑30) > 30 ML IN 1 BOTTLE, GLASS
Active Ingredients:
- Dronabinol
Dosage Strength:
- 5 mg/mL
Pharmaceutical Classes:
- Cannabinoid [EPC]
- Cannabinoids [Chemical/Ingredient]
Related Products:
Based on records with the same trade name.- 78613-201 Syndros 5 mg/ml Oral Solution by Benuvia Operations, LLC
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