71205-463 : 24 Hr Tramadol Hydrochloride 100 mg Extended Release Oral Tablet


NDC: 71205-463
Labeler: Proficient Rx Lp
Drug Name:  Tramadol Hydrochloride
Rev. Date: 
CSA Schedule: CIV (US) [1]


[1] Schedule IV Controlled Substance: Low potential for abuse relative to substances in Schedule III. Examples include Alprazolam (Xanax), Diazepam (Valium), Carisoprodol (Soma), Clonazepam (Klonopin), Lorazepam (Ativan), Clorazepate (Tranxene), Midazolam (Versed), Temazepam (Restoril), and Triazolam (Halcion).. More Details: US Dept of Justice Controlled Substance Schedules.

Appearance:


Markings: L010
Shapes:  Round
Colors:  White
Size (mm): 6
Segments: * 1

* Segments = the number of equally sized pieces which the pill can be broken into. In this case, a value of 1 indicates a solid pill with no score lines.

NDC Package Codes:

  • 71205-463-30: 30 TABLET, EXTENDED RELEASE IN 1 BOTTLE (71205‑463‑30)
  • 71205-463-60: 60 TABLET, EXTENDED RELEASE IN 1 BOTTLE (71205‑463‑60)
  • 71205-463-90: 90 TABLET, EXTENDED RELEASE IN 1 BOTTLE (71205‑463‑90)

Active Ingredients:

  • Tramadol Hydrochloride

Dosage Strength:

  • 100 mg

Inactive Ingredients:

  • Microcrystalline Cellulose
  • Dibutyl Sebacate
  • Ethylcellulose, Unspecified
  • Ferrosoferric Oxide
  • Crospovidone, Unspecified
  • Propylene Glycol
  • Shellac
  • Silicon Dioxide
  • Sodium Stearyl Fumarate /

Pharmaceutical Classes:

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

Related Products:

Based on records with the same trade name.
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  • 0093-0058 Tramadol Hydrochloride 50 mg Oral Tablet by Teva Pharmaceuticals USA Inc
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  • 0378-4151 Tramadol Hydrochloride 50 mg Oral Tablet by Mylan Pharmaceuticals Inc.
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  • 0378-4153 Tramadol Hydrochloride 200 mg Oral Tablet, Extended Release by Mylan Pharmaceuticals Inc.
  • 0378-4154 Tramadol Hydrochloride 300 mg Oral Tablet, Extended Release by Mylan Pharmaceuticals Inc.
  • 0615-7810 Tramadol Hydrochloride 50 mg Oral Tablet, Film Coated by Ncs Healthcare of Ky, Inc Dba Vangard Labs
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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.