16590-659 : Oxycodone Hydrochloride 15 mg Oral Tablet


NDC: 16590-659
Labeler: Stat Rx USA LLC
Product Type: Human Prescription Drug
Drug Name:  Oxycodone Hydrochloride
Dosage Form: Oral Tablet
Application #: ANDA077712
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: 4811;V
Shapes:  Round
Colors:  Green
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:

  • 16590-659-30: 30 TABLET IN 1 BOTTLE (16590‑659‑30)
  • 16590-659-56: 56 TABLET IN 1 BOTTLE (16590‑659‑56)
  • 16590-659-60: 60 TABLET IN 1 BOTTLE (16590‑659‑60)
  • 16590-659-62: 84 TABLET IN 1 BOTTLE (16590‑659‑62)
  • 16590-659-71: 100 TABLET IN 1 BOTTLE (16590‑659‑71)
  • 16590-659-72: 120 TABLET IN 1 BOTTLE (16590‑659‑72)
  • 16590-659-73: 112 TABLET IN 1 BOTTLE (16590‑659‑73)
  • 16590-659-82: 180 TABLET IN 1 BOTTLE (16590‑659‑82)
  • 16590-659-83: 150 TABLET IN 1 BOTTLE (16590‑659‑83)
  • 16590-659-90: 90 TABLET IN 1 BOTTLE (16590‑659‑90)

Active Ingredients:

  • Oxycodone Hydrochloride

Dosage Strength:

  • 15 mg

Inactive Ingredients:

  • Lactose Monohydrate
  • Magnesium Stearate
  • Cellulose, Microcrystalline
  • Povidone
  • Sodium Starch Glycolate Type a Potato
  • Stearic Acid
  • Fd&c Blue No. 1
  • D&c Yellow No. 10

Pharmaceutical Classes:

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

Related Products:

Based on records with the same trade name.
  • 16590-835 Oxycodone Hydrochloride 5 mg Oral Tablet by Stat Rx LLC USA
  • 42549-610 Oxycodone Hydrochloride 5 mg/1 Oral Tablet by Stat Rx USA LLC
  • 42549-643 Oxycodone Hydrochloride 15 mg Oral Tablet by Stat Rx USA LLC
  • 42549-644 Oxycodone Hydrochloride 30 mg Oral Tablet by Stat Rx USA 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
  • 0093-5734 Oxycodone Hydrochloride 80 mg Oral Tablet, Film Coated, Extended Release by Teva Pharmaceuticals USA Inc
  • 0115-1556 Oxycodone Hydrochloride 10 mg Oral Tablet, Film Coated, Extended Release by Impax Generics
  • 0115-1557 Oxycodone Hydrochloride 15 mg Oral Tablet, Film Coated, Extended Release by Impax Generics
  • 0115-1558 Oxycodone Hydrochloride 20 mg Oral Tablet, Film Coated, Extended Release by Impax Generics
  • 0115-1559 Oxycodone Hydrochloride 30 mg Oral Tablet, Film Coated, Extended Release by Impax Generics
  • 0115-1560 Oxycodone Hydrochloride 40 mg Oral Tablet, Film Coated, Extended Release by Impax Generics
  • 0115-1561 Oxycodone Hydrochloride 60 mg Oral Tablet, Film Coated, Extended Release by Impax Generics
  • 0115-1562 Oxycodone Hydrochloride 80 mg Oral Tablet, Film Coated, Extended Release by Impax Generics
  • 0121-0826 Oxycodone Hydrochloride 100 mg/5ml Oral Solution by Pharmaceutical Associates, Inc.
  • More related products ...

NDC QR Code

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NDC 16590-659 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.