55289-407 : Lorcet 10/650 (Hydrocodone / Acetaminophen) Oral Tablet

NDC:	55289-407
Labeler:	Pd-rx Pharmaceuticals, Inc.
Product Type:	Human Prescription Drug
Drug Name:	Lorcet
Dosage Form:	Oral Tablet
Application #:	ANDA081223
Rev. Date:	May 29, 1992
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:	UAB;63;50
Shapes:	Capsule
Colors:	Blue
Size (mm):	16
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:

• 55289-407-20: 20 TABLET IN 1 BOTTLE, PLASTIC (55289‑407‑20)

Active Ingredients:

• Acetaminophen
• Hydrocodone Bitartrate

Inactive Ingredients:

• Silicon Dioxide
• Croscarmellose Sodium
• Crospovidone
• Cellulose, Microcrystalline
• Povidone
• Starch, Corn
• Stearic Acid
• Fd&c Blue No. 1

Pharmaceutical Classes:

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

Related Products:

Based on records with the same trade name.

• 51862-585 Lorcet Oral Tablet by Mayne Pharma Inc.
• 55154-7301 Lorcet 10/650 (Hydrocodone / Acetaminophen) Oral Tablet by Cardinal Health
• 68308-221 Lorcet Oral Tablet by Midlothian Laboratories
• 68308-224 Lorcet Oral Tablet by Mayne Pharma

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