prednisolone sodium phosphate

Generic: prednisolone sodium phosphate

Labeler: bausch & lomb incorporated
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name prednisolone sodium phosphate
Generic Name prednisolone sodium phosphate
Labeler bausch & lomb incorporated
Dosage Form SOLUTION/ DROPS
Routes
OPHTHALMIC
Active Ingredients

prednisolone sodium phosphate 10 mg/mL

Manufacturer
Bausch & Lomb Incorporated

Identifiers & Regulatory

Product NDC 24208-715
Product ID 24208-715_87bea906-f7cf-4987-abb2-02981b5ea0e2
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA040070
Listing Expiration 2026-12-31
Marketing Start 1994-07-29

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 24208715
Hyphenated Format 24208-715

Supplemental Identifiers

RxCUI
314165
UNII
IV021NXA9J

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 prednisolone sodium phosphate (source: ndc)
Generic Name prednisolone sodium phosphate (source: ndc)
Application Number ANDA040070 (source: ndc)
Routes
OPHTHALMIC
source: ndc

Resolved Composition

Strengths
  • 10 mg/mL
source: ndc
Packaging
  • 1 BOTTLE, DROPPER in 1 CARTON (24208-715-10) / 10 mL in 1 BOTTLE, DROPPER
source: ndc

Packages (1)

Ingredients (1)

prednisolone sodium phosphate (10 mg/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["OPHTHALMIC"], "spl_id": "87bea906-f7cf-4987-abb2-02981b5ea0e2", "openfda": {"unii": ["IV021NXA9J"], "rxcui": ["314165"], "spl_set_id": ["8a7f0f2a-3a48-4488-89cd-3e91c3b1365f"], "manufacturer_name": ["Bausch & Lomb Incorporated"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, DROPPER in 1 CARTON (24208-715-10)  / 10 mL in 1 BOTTLE, DROPPER", "package_ndc": "24208-715-10", "marketing_start_date": "19990729"}], "brand_name": "PREDNISOLONE SODIUM PHOSPHATE", "product_id": "24208-715_87bea906-f7cf-4987-abb2-02981b5ea0e2", "dosage_form": "SOLUTION/ DROPS", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "24208-715", "generic_name": "PREDNISOLONE SODIUM PHOSPHATE", "labeler_name": "Bausch & Lomb Incorporated", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PREDNISOLONE SODIUM PHOSPHATE", "active_ingredients": [{"name": "PREDNISOLONE SODIUM PHOSPHATE", "strength": "10 mg/mL"}], "application_number": "ANDA040070", "marketing_category": "ANDA", "marketing_start_date": "19940729", "listing_expiration_date": "20261231"}