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Lorcet Plus - 0785-1122-01 - (hydrocodone bitartrate and acetaminophen)

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Drug Information of Lorcet Plus

Product NDC: 0785-1122
Proprietary Name: Lorcet Plus
Non Proprietary Name: hydrocodone bitartrate and acetaminophen
Active Ingredient(s): 650; 7.5    mg/1; mg/1 & nbsp;   hydrocodone bitartrate and acetaminophen
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Lorcet Plus

Product NDC: 0785-1122
Labeler Name: Forest Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA089689
Marketing Category: ANDA
Start Marketing Date: 19841231

Package Information of Lorcet Plus

Package NDC: 0785-1122-01
Package Description: 100 TABLET in 1 BOTTLE, PLASTIC (0785-1122-01)

NDC Information of Lorcet Plus

NDC Code 0785-1122-01
Proprietary Name Lorcet Plus
Package Description 100 TABLET in 1 BOTTLE, PLASTIC (0785-1122-01)
Product NDC 0785-1122
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name hydrocodone bitartrate and acetaminophen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19841231
Marketing Category Name ANDA
Labeler Name Forest Laboratories, Inc.
Substance Name ACETAMINOPHEN; HYDROCODONE BITARTRATE
Strength Number 650; 7.5
Strength Unit mg/1; mg/1
Pharmaceutical Classes Opioid Agonist [EPC],Opioid Agonists [MoA]

Complete Information of Lorcet Plus


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