pred forte

Generic: prednisolone acetate

Labeler: allergan, inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name pred forte
Generic Name prednisolone acetate
Labeler allergan, inc.
Dosage Form SUSPENSION/ DROPS
Routes
OPHTHALMIC
Active Ingredients

prednisolone acetate 10 mg/mL

Manufacturer
Allergan, Inc.

Identifiers & Regulatory

Product NDC 11980-180
Product ID 11980-180_bff1726c-7781-49de-8a61-bc37a755c92b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA017011
Marketing Start 1973-06-01
Marketing End 2027-05-31

Pharmacologic Class

Classes
corticosteroid hormone receptor agonists [moa] corticosteroid [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 11980180
Hyphenated Format 11980-180

Supplemental Identifiers

RxCUI
1376336 1548724
UPC
0311980180058 0311980180157 0311980180102
UNII
8B2807733D

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name pred forte (source: ndc)
Generic Name prednisolone acetate (source: ndc)
Application Number NDA017011 (source: ndc)
Routes
OPHTHALMIC
source: ndc

Resolved Composition

Strengths
  • 10 mg/mL
source: ndc
Packaging
  • 1 BOTTLE, DROPPER in 1 CARTON (11980-180-05) / 5 mL in 1 BOTTLE, DROPPER
  • 1 BOTTLE, DROPPER in 1 CARTON (11980-180-10) / 10 mL in 1 BOTTLE, DROPPER
  • 1 BOTTLE, DROPPER in 1 CARTON (11980-180-15) / 15 mL in 1 BOTTLE, DROPPER
source: ndc

Packages (3)

Ingredients (1)

prednisolone acetate (10 mg/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["OPHTHALMIC"], "spl_id": "bff1726c-7781-49de-8a61-bc37a755c92b", "openfda": {"upc": ["0311980180058", "0311980180157", "0311980180102"], "unii": ["8B2807733D"], "rxcui": ["1376336", "1548724"], "spl_set_id": ["00a5aa88-e361-4ea7-8922-530c738b726e"], "manufacturer_name": ["Allergan, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, DROPPER in 1 CARTON (11980-180-05)  / 5 mL in 1 BOTTLE, DROPPER", "package_ndc": "11980-180-05", "marketing_end_date": "20270531", "marketing_start_date": "19730601"}, {"sample": false, "description": "1 BOTTLE, DROPPER in 1 CARTON (11980-180-10)  / 10 mL in 1 BOTTLE, DROPPER", "package_ndc": "11980-180-10", "marketing_end_date": "20260831", "marketing_start_date": "19730601"}, {"sample": false, "description": "1 BOTTLE, DROPPER in 1 CARTON (11980-180-15)  / 15 mL in 1 BOTTLE, DROPPER", "package_ndc": "11980-180-15", "marketing_end_date": "20260430", "marketing_start_date": "19730601"}], "brand_name": "PRED FORTE", "product_id": "11980-180_bff1726c-7781-49de-8a61-bc37a755c92b", "dosage_form": "SUSPENSION/ DROPS", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "11980-180", "generic_name": "prednisolone acetate", "labeler_name": "Allergan, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PRED FORTE", "active_ingredients": [{"name": "PREDNISOLONE ACETATE", "strength": "10 mg/mL"}], "application_number": "NDA017011", "marketing_category": "NDA", "marketing_end_date": "20270531", "marketing_start_date": "19730601"}