prednisolone sodium phosphate
Generic: prednisolone sodium phosphate
Labeler: bausch & lomb incorporatedDrug Facts
Product Profile
Brand Name
prednisolone sodium phosphate
Generic Name
prednisolone sodium phosphate
Labeler
bausch & lomb incorporated
Dosage Form
SOLUTION/ DROPS
Routes
Active Ingredients
prednisolone sodium phosphate 10 mg/mL
Manufacturer
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
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
24208715
Hyphenated Format
24208-715
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
source: ndc
Resolved Composition
Strengths
- 10 mg/mL
Packaging
- 1 BOTTLE, DROPPER in 1 CARTON (24208-715-10) / 10 mL in 1 BOTTLE, DROPPER
Packages (1)
Ingredients (1)
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"}