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CELESTONE SOLUSPAN - 49349-757-01 - (Betamethasone Acetate and Betamethasone Sodium Phosphate)

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Drug Information of CELESTONE SOLUSPAN

Product NDC: 49349-757
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): INTRAMUSCULAR
Dosage Form(s): INJECTION, SUSPENSION
Coding System: National Drug Codes(NDC)

Labeler Information of CELESTONE SOLUSPAN

Product NDC: 49349-757
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA014602
Marketing Category: NDA
Start Marketing Date: 20130610

Package Information of CELESTONE SOLUSPAN

Package NDC: 49349-757-01
Package Description: 5 mL in 1 VIAL (49349-757-01)

NDC Information of CELESTONE SOLUSPAN

NDC Code 49349-757-01
Proprietary Name CELESTONE SOLUSPAN
Package Description 5 mL in 1 VIAL (49349-757-01)
Product NDC 49349-757
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Betamethasone Acetate and Betamethasone Sodium Phosphate
Dosage Form Name INJECTION, SUSPENSION
Route Name INTRAMUSCULAR
Start Marketing Date 20130610
Marketing Category Name NDA
Labeler Name REMEDYREPACK INC.
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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