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CELESTONE SOLUSPAN - 0085-0566-05 - (Betamethasone Acetate and Betamethasone Sodium Phosphate)

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Drug Information of CELESTONE SOLUSPAN

Product NDC: 0085-0566
Proprietary Name: CELESTONE SOLUSPAN
Non Proprietary Name: Betamethasone Acetate and Betamethasone Sodium Phosphate
Active Ingredient(s): 3; 3    mg/mL; mg/mL & nbsp;   Betamethasone Acetate and Betamethasone Sodium Phosphate
Administration Route(s): INTRA-ARTICULAR; INTRALESIONAL; INTRAMUSCULAR; SOFT TISSUE
Dosage Form(s): INJECTION, SUSPENSION
Coding System: National Drug Codes(NDC)

Labeler Information of CELESTONE SOLUSPAN

Product NDC: 0085-0566
Labeler Name: Merck Sharp & Dohme Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA014602
Marketing Category: NDA
Start Marketing Date: 19650315

Package Information of CELESTONE SOLUSPAN

Package NDC: 0085-0566-05
Package Description: 1 VIAL, MULTI-DOSE in 1 BOX (0085-0566-05) > 5 mL in 1 VIAL, MULTI-DOSE

NDC Information of CELESTONE SOLUSPAN

NDC Code 0085-0566-05
Proprietary Name CELESTONE SOLUSPAN
Package Description 1 VIAL, MULTI-DOSE in 1 BOX (0085-0566-05) > 5 mL in 1 VIAL, MULTI-DOSE
Product NDC 0085-0566
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Betamethasone Acetate and Betamethasone Sodium Phosphate
Dosage Form Name INJECTION, SUSPENSION
Route Name INTRA-ARTICULAR; INTRALESIONAL; INTRAMUSCULAR; SOFT TISSUE
Start Marketing Date 19650315
Marketing Category Name NDA
Labeler Name Merck Sharp & Dohme Corp.
Substance Name BETAMETHASONE ACETATE; BETAMETHASONE SODIUM PHOSPHATE
Strength Number 3; 3
Strength Unit mg/mL; mg/mL
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA],Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of CELESTONE SOLUSPAN


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