prednisolone acetate

Generic: prednisolone acetate

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name prednisolone acetate
Generic Name prednisolone acetate
Labeler a-s medication solutions
Dosage Form SUSPENSION/ DROPS
Routes
OPHTHALMIC
Active Ingredients

prednisolone acetate 10 mg/mL

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-7539
Product ID 50090-7539_af502300-c29e-405b-bb6f-f125d432a2c1
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA216935
Listing Expiration 2027-12-31
Marketing Start 2024-10-11

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500907539
Hyphenated Format 50090-7539

Supplemental Identifiers

RxCUI
1376336
UNII
8B2807733D

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 acetate (source: ndc)
Generic Name prednisolone acetate (source: ndc)
Application Number ANDA216935 (source: ndc)
Routes
OPHTHALMIC
source: ndc

Resolved Composition

Strengths
  • 10 mg/mL
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (50090-7539-0) / 5 mL in 1 BOTTLE
source: ndc

Packages (1)

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": "af502300-c29e-405b-bb6f-f125d432a2c1", "openfda": {"unii": ["8B2807733D"], "rxcui": ["1376336"], "spl_set_id": ["f0e1b691-73ff-49ee-8a3c-71769b284ab8"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (50090-7539-0)  / 5 mL in 1 BOTTLE", "package_ndc": "50090-7539-0", "marketing_start_date": "20250422"}], "brand_name": "PREDNISOLONE ACETATE", "product_id": "50090-7539_af502300-c29e-405b-bb6f-f125d432a2c1", "dosage_form": "SUSPENSION/ DROPS", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "50090-7539", "generic_name": "prednisolone acetate", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PREDNISOLONE ACETATE", "active_ingredients": [{"name": "PREDNISOLONE ACETATE", "strength": "10 mg/mL"}], "application_number": "ANDA216935", "marketing_category": "ANDA", "marketing_start_date": "20241011", "listing_expiration_date": "20271231"}