0093-1151 : Fentanyl 200 ug/1 Buccal; Sublingual Tablet


NDC: 0093-1151
Labeler: Teva Pharmaceuticals USA, Inc.
Product Type: Human Prescription Drug
Drug Name:  Fentanyl
Dosage Form: Buccal; Sublingual Tablet
Application #: NDA021947
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: C;2
Shapes:  Round
Colors:  White
Size (mm): 8
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:

  • 0093-1151-28: 28 BLISTER PACK IN 1 CARTON (0093‑1151‑28) > 1 TABLET IN 1 BLISTER PACK (0093‑1151‑19)

Active Ingredients:

  • Fentanyl Citrate

Dosage Strength:

  • 200 ug/1

Inactive Ingredients:

  • Mannitol
  • Sodium Starch Glycolate Type a Potato
  • Sodium Bicarbonate
  • Sodium Carbonate
  • Anhydrous Citric Acid
  • Magnesium Stearate /

Pharmaceutical Classes:

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

Related Products:

Based on records with the same trade name.
  • 0093-1150 Fentanyl 100 ug/1 Buccal; Sublingual Tablet by Teva Pharmaceuticals USA, Inc.
  • 0093-1153 Fentanyl 400 ug/1 Buccal; Sublingual Tablet by Teva Pharmaceuticals USA, Inc.
  • 0093-1154 Fentanyl 600 ug/1 Buccal; Sublingual Tablet by Teva Pharmaceuticals USA, Inc.
  • 0093-1155 Fentanyl 800 ug/1 Buccal; Sublingual Tablet by Teva Pharmaceuticals USA, Inc.
  • 0093-6900 Fentanyl 25 ug/H Transdermal Patch, Extended Release by Teva Pharmaceuticals USA Inc
  • 0093-6901 Fentanyl 50 ug/H Transdermal Patch, Extended Release by Teva Pharmaceuticals USA Inc
  • 0093-6902 Fentanyl 75 ug/H Transdermal Patch, Extended Release by Teva Pharmaceuticals USA Inc
  • 0093-6903 Fentanyl 100 ug/H Transdermal Patch, Extended Release by Teva Pharmaceuticals USA Inc
  • 0245-0420 Fentanyl 25 ug/H Transdermal Patch, Extended Release by Upsher-smith Laboratories, Inc.
  • 0245-0421 Fentanyl 50 ug/H Transdermal Patch, Extended Release by Upsher-smith Laboratories, Inc.
  • 0245-0422 Fentanyl 75 ug/H Transdermal Patch, Extended Release by Upsher-smith Laboratories, Inc.
  • 0245-0423 Fentanyl 100 ug/H Transdermal Patch, Extended Release by Upsher-smith Laboratories, Inc.
  • 0378-9119 Fentanyl 12 ug/H Transdermal Patch by Mylan Pharmaceuticals Inc.
  • 0378-9121 Fentanyl 25 ug/H Transdermal Patch by Mylan Pharmaceuticals Inc.
  • 0378-9122 Fentanyl 50 ug/H Transdermal Patch by Mylan Pharmaceuticals Inc.
  • 0378-9123 Fentanyl 75 ug/H Transdermal Patch by Mylan Pharmaceuticals Inc.
  • 0378-9124 Fentanyl 100 ug/H Transdermal Patch by Mylan Pharmaceuticals Inc.
  • 0378-9125 Fentanyl 37.5 ug/H Transdermal Patch by Mylan Pharmaceuticals Inc.
  • 0378-9126 Fentanyl 62.5 ug/H Transdermal Patch by Mylan Pharmaceuticals Inc.
  • 0378-9127 Fentanyl 87.5 ug/H Transdermal Patch by Mylan Pharmaceuticals Inc.
  • More related products ...

NDC QR Code

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NDC 0093-1151 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.