Prednisolone Sodium Phosphate

Labeler
ATLANTIC BIOLOGICALS CORP.
Dosage Form
SOLUTION
Route
ORAL
NDCs
17856-0759-5, 17856-0759-7, 17856-0759-4, 17856-0759-8, 17856-0759-1, 17856-0759-3, 17856-0759-2, 17856-0759-6
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Active Ingredients

Display Name UNII Strength
Prednisolone Sodium Phosphate IV021NXA9J 15 mg/5 mL

Matched Sugar Alcohols

No sugar alcohol excipients matched in local index.

Inactive Ingredients

Display Name UNII
Corn Syrup 9G5L16BK6N
Edetate Disodium 7FLD91C86K
Glycerin PDC6A3C0OX
Hydroxyethyl Cellulose (140 Mpa.s At 5%) 8136Y38GY5
Methylparaben A2I8C7HI9T
Potassium Phosphate, Dibasic CI71S98N1Z
Potassium Phosphate, Monobasic 4J9FJ0HL51
Water 059QF0KO0R
Saccharin Sodium SB8ZUX40TY