0785-6350 : Lorcet 10/650 (Hydrocodone / Acetaminophen) Oral Tablet

NDC:	0785-6350
Labeler:	Forest Laboratories, Inc.
Product Type:	Human Prescription Drug
Drug Name:	Lorcet 10/650
Dosage Form:	Oral Tablet
Application #:	ANDA081223
Rev. Date:	Dec 31, 1984
CSA Schedule:	CIII (US) [1]

^[1] Schedule III / IIIN Controlled Substance: Has a potential for abuse less than substances in Schedules I or II and abuse may lead to moderate or low physical dependence or high psychological dependence. (i.e. Products containing not more than 90 milligrams of Codeine per dosage unit [such as Tylenol with Codeine], other narcotics such as Buprenorphine (Suboxone), and Schedule IIIN non-narcotics such as Didrex, Ketamine, Phendimetrazine, and Anabolic Steroids). More Details: US Dept of Justice Controlled Substance Schedules.

Appearance:

Markings:	UAD;6350
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:

• 0785-6350-01: 100 TABLET IN 1 BOTTLE, PLASTIC (0785‑6350‑01)
• 0785-6350-50: 500 TABLET IN 1 BOTTLE, PLASTIC (0785‑6350‑50)

Active Ingredients:

• Acetaminophen
• Hydrocodone Bitartrate

Inactive Ingredients:

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

Pharmaceutical Classes:

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

Related Products:

Based on records with the same trade name.

• 65084-266 Lorcet 10/650 (Hydrocodone / Acetaminophen) Oral Tablet by Rx Pak Division of Mckesson Corporation

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