0472-1030 : Hydromet Oral Syrup


NDC0472-1030
Labeler: Actavis Mid Atlantic LLC
Product Type: Human Prescription Drug
Drug Name:  Hydromet
Dosage Form: Oral Syrup
Application #: ANDA088017
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:

  • 0472-1030-16: 473 ML IN 1 BOTTLE (0472‑1030‑16)

Active Ingredients:

  • Hydrocodone Bitartrate
  • Homatropine Methylbromide

Dosage Strength:

  • 5 mg/5mL
  • 1.5 mg/5mL

Pharmaceutical Classes:

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

NDC QR Code

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NDC 0472-1030 QR Code

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