JTT PHYSICIANS JOINT, TUNNEL AND TRIGGER- triamcinolone acetonide,lidocaine hydrochloride, povidone iodine, ammonia kit

País: Estados Unidos

Língua: inglês

Origem: NLM (National Library of Medicine)

Ingredientes ativos:

TRIAMCINOLONE ACETONIDE (UNII: F446C597KA) (TRIAMCINOLONE ACETONIDE - UNII:F446C597KA)

Disponível em:

RX PHARMA-PACK, INC.

DCI (Denominação Comum Internacional):

TRIAMCINOLONE ACETONIDE

Composição:

TRIAMCINOLONE ACETONIDE 40 mg in 1 mL

Tipo de prescrição:

PRESCRIPTION DRUG

Indicações terapêuticas:

Intramuscular Where oral therapy is not feasible, injectable corticosteroid therapy, including Kenalog-40 Injection and Kenalog-80 Injection (triamcinolone acetonide injectable suspension, USP) are indicated for intramuscular use as follows: Allergic states : Control of severe or incapacitating allergic conditions intractable to adequate trials of conventional treatment in asthma, atopic dermatitis, contact dermatitis, drug hypersensitivity reactions, perennial or seasonal allergic rhinitis, serum sickness, transfusion reactions. Dermatologic diseases : Bullous dermatitis herpetiformis, exfoliative erythroderma, mycosis fungoides, pemphigus, severe erythema multiforme (Stevens-Johnson syndrome). Endocrine disorders : Primary or secondary adrenocortical insufficiency (hydrocortisone or cortisone is the drug of choice; synthetic analogs may be used in conjunction with mineralocorticoids where applicable; in infancy, mineralocorticoid supplementation is of particular importance), congenital adrenal hyperpl

Resumo do produto:

Kenalog® -40 Injection (triamcinolone acetonide injectable suspension, USP) is supplied in vials providing 40 mg triamcinolone acetonide per mL. Kenalog® -80 Injection (triamcinolone acetonide injectable suspension, USP) is supplied in vials providing 80 mg triamcinolone acetonide per mL. Storage Store at controlled room temperature, 20° to 25°C (68° to 77°F); protect from temperatures below 20°C (68°F). Store vial in carton to protect from light. Store vial upright. Bristol-Myers Squibb Company Princeton, NJ 08543 USA 1374114A0 Revised: April 2019 Lidocaine Hydrochloride Injection, USP is supplied as follows: Single-dose products are preservative-free. Store at 20 to 25°C (68 to 77°F). [see USP Controlled Room Temperature.] Lidocaine Hydrochloride Injection, USP solutions packaged in ampuls and glass teartop vials may be autoclaved one time only. Autoclave at 15 pounds pressure, 121ºC (250ºF) for 15 minutes. DO NOT AUTOCLAVE PRODUCT IN PLASTIC VIALS. Distributed by Hospira, Inc., Lake Forest, IL 60045 USA LAB-1118-4.0 02/2019

Status de autorização:

New Drug Application

Características técnicas

JTT PHYSICIANS JOINT, TUNNEL AND TRIGGER- TRIAMCINOLONE
ACETONIDE,LIDOCAINE
HYDROCHLORIDE, POVIDONE IODINE, AMMONIA
RX PHARMA-PACK, INC.
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NOT FOR USE IN NEONATES
CONTAINS BENZYL ALCOHOL
FOR INTRAMUSCULAR OR INTRA-ARTICULAR USE ONLY
NOT FOR INTRAVENOUS, INTRADERMAL, INTRAOCULAR, EPIDURAL, OR
INTRATHECAL USE
KENALOG-40 INJECTION - TRIAMCINOLONE ACETONIDE INJECTION, SUSPENSION
KENALOG -40 INJECTION
(TRIAMCINOLONE ACETONIDE INJECTABLE SUSPENSION, USP)
E.R. SQUIBB & SONS, L.L.C.
NOT FOR USE IN NEONATES
CONTAINS BENZYL ALCOHOL
FOR INTRAMUSCULAR OR INTRA-ARTICULAR USE ONLY
NOT FOR INTRAVENOUS, INTRADERMAL, INTRAOCULAR, EPIDURAL, OR
INTRATHECAL USE
DESCRIPTION
Kenalog
-40 Injection and Kenalog
-80 Injection (triamcinolone acetonide injectable suspension, USP)
are a synthetic glucocorticoid corticosteroid with anti-inflammatory
action. THESE FORMULATIONS
ARE SUITABLE FOR INTRAMUSCULAR AND INTRA-ARTICULAR USE ONLY. THESE
FORMULATIONS ARE NOT FOR INTRADERMAL INJECTION.
Kenalog
-40 Injection: Each mL of the sterile aqueous suspension provides 40
mg triamcinolone
acetonide, with 0.66% sodium chloride for isotonicity, 0.99% (w/v)
benzyl alcohol as a preservative,
0.63% carboxymethylcellulose sodium, and 0.04% polysorbate 80. Sodium
hydroxide or hydrochloric
acid may be present to adjust pH to 5.0 to 7.5. At the time of
manufacture, the air in the container is
replaced by nitrogen.
Kenalog
-80 Injection: Each mL of the sterile aqueous suspension provides 80
mg triamcinolone
acetonide, with 0.66% sodium chloride for isotonicity, 0.99% (w/v)
benzyl alcohol as a preservative,
0.63% carboxymethylcellulose sodium, and 0.04% polysorbate 80. Sodium
hydroxide or hydrochloric
acid may be present to adjust pH to 5.0 to 7.5. At the time of
manufacture, the air in the container is
replaced by nitrogen.
The chemical name for triamcinolone acetonide is 9-Fluoro-11β,
6α,17,21-tetrahydroxypregna-1,4-
diene-3,20-dione cyclic 16,17-acetal with acetone. Its structural
formula is:
TRIAMCINOLONE ACETONIDE STRUCTURAL FORMULA
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