PRED FORTE 10 mg/mL
prednisolone acetate · SUSPENSION/ DROPS · Allergan, Inc.
No Recall History
Plain English
PRED FORTE is a suspension/ drops containing prednisolone acetate at 10 mg/mL, taken ophthalmic. Manufactured by Allergan, Inc..
Key Facts
- Brand Name
- PRED FORTE
- Generic Name
- prednisolone acetate
- NDC Code (Product)
11980-180- Manufacturer
- Allergan, Inc.
- Strength
- 10 mg/mL
- Dosage Form
- SUSPENSION/ DROPS
- Route
- OPHTHALMIC
- Marketing Status
- Application #
- NDA017011
- Marketing Start
- 06/01/1973
Recall History
No Recall HistoryFrequently Asked Questions
What is PRED FORTE used for?
PRED FORTE contains prednisolone acetate. It is a suspension/ drops taken ophthalmic. Consult your doctor for specific uses.
Is PRED FORTE a controlled substance?
PRED FORTE is not classified as a controlled substance by the DEA.
What is the generic name for PRED FORTE?
The generic name for PRED FORTE is prednisolone acetate. There are 11 other brand versions of prednisolone acetate.
What is the NDC code for PRED FORTE 10 mg/mL?
The NDC (National Drug Code) for PRED FORTE 10 mg/mL is 11980-180, listed by Allergan, Inc..
Other Prednisolone Brands
See all →- PREDNISOLONE ACETATE10 mg/mL85766-124
- PREDNISOLONE ACETATE10 mg/mL50090-7539
- PREDNISOLONE ACETATE10 mg/mL67296-2176
- PRED MILD1.2 mg/mL11980-174
- PREDNISOLONE ACETATE10 mg/mL50090-1912
- Prednisolone Acetate10 mg/mL61314-637
- prednisolone acetate10 mg/mL60219-2550
- prednisolone acetate10 mg/mL60219-2552
- PREDNISOLONE ACETATE10 mg/mL50090-5275
- PREDNISOLONE ACETATE10 mg/mL60758-119
Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.
Data from openFDA · Public domain (CC0 1.0)