0093-6900 : Fentanyl 25 ug/H Transdermal Patch, Extended Release

NDC:	0093-6900
Labeler:	Teva Pharmaceuticals USA Inc
Product Type:	Human Prescription Drug
Drug Name:	Fentanyl
Dosage Form:	Transdermal Patch, Extended Release
Application #:	ANDA077449
Rev. Date:	Dec 22, 2008
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:

0093-6900-45: 5 BLISTER PACK IN 1 CARTON (0093‑6900‑45) > 1 PATCH IN 1 BLISTER PACK (0093‑6900‑19) > 72 H IN 1 PATCH

Active Ingredients:

Fentanyl

Dosage Strength:

25 ug/h

Pharmaceutical Classes:

Full Opioid Agonists [MoA]
Opioid Agonist [EPC]

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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.