21724-701 : Procentra 5 mg/5ml Oral Solution


NDC: 21724-701
Labeler: Independence Pharmaceuticals, LLC
Product Type: Human Prescription Drug
Drug Name: Procentra
Dosage Form: Oral Solution
Application #: ANDA040776
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:

  • 21724-701-05: 473 ML IN 1 BOTTLE, PLASTIC (21724‑701‑05)

Active Ingredients:

  • Dextroamphetamine Sulfate

Dosage Strength:

  • 5 mg/5mL

Pharmaceutical Classes:

  • Central Nervous System Stimulant [EPC]
  • Central Nervous System Stimulation [PE]

Related Products:

Based on records with the same trade name.
  • 13551-701 Procentra 5 mg/5ml Oral Liquid by Fsc Laboratories, Inc

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.