55700-020 : Oxycodone Hydrochloride 10 mg Oral Tablet


NDC55700-020
Labeler: Lake Erie Medical Dba Quality Care Products LLC
Product Type: Human Prescription Drug
Drug Name:  Oxycodone Hydrochloride
Dosage Form: Oral Tablet
Application #: ANDA090659
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.

Appearance:


Markings: 370
Shapes:  Round
Colors:  Pink
Size (mm): 6
Segments: * 2

* Segments = the number of equally sized pieces which the pill can be broken into. In this case, a value of 2 indicates a scored pill which can be broken into 2 equal pieces.

NDC Package Codes:

  • 55700-020-30: 30 TABLET IN 1 BOTTLE (55700‑020‑30)
  • 55700-020-60: 60 TABLET IN 1 BOTTLE (55700‑020‑60)
  • 55700-020-90: 90 TABLET IN 1 BOTTLE (55700‑020‑90)

Active Ingredients:

  • Oxycodone Hydrochloride

Dosage Strength:

  • 10 mg

Inactive Ingredients:

  • Anhydrous Lactose
  • Silicon Dioxide
  • Magnesium Stearate
  • Cellulose, Microcrystalline
  • Starch, Corn
  • Sodium Starch Glycolate Type a Potato
  • D&c Red No. 27
  • D&c Red No. 30

Pharmaceutical Classes:

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

Related Products:

Based on records with the same trade name.
  • 55700-174 Oxycodone Hydrochloride 15 mg Oral Tablet by Lake Erie Medical Dba Quality Care Products LLC
  • 55700-175 Oxycodone Hydrochloride 30 mg Oral Tablet by Lake Erie Medical Dba Quality Care Products LLC
  • 55700-334 Oxycodone Hydrochloride 10 mg Oral Tablet, Film Coated, Extended Release by Lake Erie Medical Dba Quality Care Products LLC
  • 55700-427 Oxycodone Hydrochloride 40 mg Oral Tablet, Film Coated, Extended Release by Lake Erie Medical Dba Quality Care Products LLC
  • 55700-431 Oxycodone Hydrochloride 20 mg Oral Tablet, Film Coated, Extended Release by Lake Erie Medical Dba Quality Care Products LLC
  • 55700-437 Oxycodone Hydrochloride 10 mg Oral Tablet, Film Coated, Extended Release by Lake Erie Medical Dba Quality Care Products LLC
  • 55700-443 Oxycodone Hydrochloride 40 mg Oral Tablet, Film Coated, Extended Release by Lake Erie Medical Dba Quality Care Products LLC
  • 55700-462 Oxycodone Hydrochloride 60 mg Oral Tablet, Film Coated, Extended Release by Lake Erie Medical Dba Quality Care Products LLC
  • 55700-509 Oxycodone Hydrochloride 20 mg Oral Tablet by Lake Erie Medical Dba Quality Care Products LLC
  • 35356-828 Oxycodone Hydrochloride 5 mg Oral Tablet by Lake Erie Medical Dba Quality Care Products LLC
  • 35356-829 Oxycodone Hydrochloride 15 mg Oral Tablet by Lake Erie Medical Dba Quality Care Products LLC
  • 35356-830 Oxycodone Hydrochloride 30 mg Oral Tablet by Lake Erie Medical Dba Quality Care Products LLC
  • 49999-851 Oxycodone Hydrochloride 30 mg Oral Tablet by Lake Erie Medical Dba Quality Care Products LLC
  • 0054-0390 Oxycodone Hydrochloride 5 mg/5ml Oral Solution by Roxane Laboratories, Inc.
  • 0054-0393 Oxycodone Hydrochloride 100 mg/5ml Oral Solution by Roxane Laboratories, Inc.
  • 0054-0522 Oxycodone Hydrochloride 100 mg/5ml Oral Solution by Roxane Laboratories, Inc.
  • 0054-0523 Oxycodone Hydrochloride 5 mg/5ml Oral Solution by Roxane Laboratories, Inc.
  • 0093-5731 Oxycodone Hydrochloride 10 mg Oral Tablet, Film Coated, Extended Release by Teva Pharmaceuticals USA Inc
  • 0093-5732 Oxycodone Hydrochloride 20 mg Oral Tablet, Film Coated, Extended Release by Teva Pharmaceuticals USA Inc
  • 0093-5733 Oxycodone Hydrochloride 40 mg Oral Tablet, Film Coated, Extended Release by Teva Pharmaceuticals USA Inc
  • More related products ...

NDC QR Code

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NDC 55700-020 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.