0641-6020 : Duramorph .5 mg/ml Epidural; Intrathecal; Intravenous Injection


NDC0641-6020
Labeler: West-ward Pharmaceutical Corp.
Product Type: Human Prescription Drug
Drug Name:  Duramorph
Dosage Form: Epidural; Intrathecal; Intravenous Injection
Application #: NDA018565
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:

  • 0641-6020-10: 10 AMPULE IN 1 CARTON (0641‑6020‑10) > 10 ML IN 1 AMPULE (0641‑6020‑01)

Active Ingredients:

  • Morphine Sulfate

Dosage Strength:

  • .5 mg/mL

Pharmaceutical Classes:

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

Related Products:

Based on records with the same trade name.
  • 0641-6019 Duramorph 1 mg/ml Epidural; Intrathecal; Intravenous Injection by West-ward Pharmaceutical Corp.
  • 60977-016 Duramorph .5 mg/ml Epidural; Intrathecal; Intravenous Injection, Solution by Baxter Healthcare Corporation
  • 60977-017 Duramorph 1 mg/ml Epidural; Intrathecal; Intravenous Injection, Solution by Baxter Healthcare Corporation

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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.