药物信息为Liquicet™ Oral Solution (hydrocodone bitartrate and acetaminophen oral solution) 10 mg/500 mg per 15 mL (Mallinckrodt Inc): DESCRIPTION
- DESCRIPTION
- CLINICAL PHARMACOLOGY
- INDICATIONS AND USAGE
- CONTRAINDICATIONS
- ADVERSE REACTIONS
- OVERDOSAGE
- DOSAGE AND ADMINISTRATION
- HOW SUPPLIED
- 外部链接相关的Liquicet™ Oral Solution (hydrocodone bitartrate and acetaminophen oral solution) 10 mg/500 mg per 15 mL (Mallinckrodt Inc)
Liquicet™ Oral Solution (hydrocodone bitartrate and acetaminophen oral solution) is supplied in liquid form for oral administration.
WARNING: May be habit forming (see PRECAUTIONS, Information for Patients, and DRUG ABUSE AND DEPENDENCE).
Hydrocodone bitartrate is an opioid analgesic and antitussive and occurs as fine, white crystals or as a crystalline powder. It is affected by light. The chemical name is: 4,5α-Epoxy-3-methoxy-17-methylmorphinan-6-one tartrate (1:1) hydrate (2:5). It has the following structural formula:

Acetaminophen, 4'-hydroxyacetanilide, a slightly bitter, white, odorless, crystalline powder, is a non-opiate, non-salicylate analgesic and antipyretic. It has the following structural formula:

Liquicet™ Oral Solution contains:
Per 5 mL Per 15 mL
Hydrocodone Bitartrate USP . . . . . . 3.33 mg 10 mg
Acetaminophen USP . . . . . . . . . . . . . 167 mg 500 mg
In addition, the liquid contains the following inactive ingredients: Citric Acid Anhydrous USP, Glycerin USP, Monoammonium Glycyrrhizinate dispersed in Glycerine, Polyethylene Glycol NF, Propylene Glycol USP, Purified Water USP, Saccharin Sodium USP, Sodium Benzoate NF, Sodium Citrate Dihydrate USP, Sorbitol Solution USP, Sucrose NF, with D&C Red #33 as coloring and artificial flavoring.
- Drug Information Provided by National Library of Medicine (NLM).
