prednisolone sodium phosphate

Generic: prednisolone sodium phosphate

Labeler: amneal pharmaceuticals ny llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name prednisolone sodium phosphate
Generic Name prednisolone sodium phosphate
Labeler amneal pharmaceuticals ny llc
Dosage Form SOLUTION
Routes
ORAL
Active Ingredients

prednisolone sodium phosphate 15 mg/5mL

Manufacturer
Amneal Pharmaceuticals NY LLC

Identifiers & Regulatory

Product NDC 69238-2122
Product ID 69238-2122_c2b9ec45-c2e4-4b1e-897e-2ed95618d56e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA216715
Listing Expiration 2026-12-31
Marketing Start 2022-10-27

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 692382122
Hyphenated Format 69238-2122

Supplemental Identifiers

RxCUI
283077
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 ANDA216715 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 15 mg/5mL
source: ndc
Packaging
  • 237 mL in 1 BOTTLE (69238-2122-9)
source: ndc

Packages (1)

Ingredients (1)

prednisolone sodium phosphate (15 mg/5mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "c2b9ec45-c2e4-4b1e-897e-2ed95618d56e", "openfda": {"unii": ["IV021NXA9J"], "rxcui": ["283077"], "spl_set_id": ["286a6032-41de-435a-b6e6-14052b66b85d"], "manufacturer_name": ["Amneal Pharmaceuticals NY LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "237 mL in 1 BOTTLE (69238-2122-9)", "package_ndc": "69238-2122-9", "marketing_start_date": "20221027"}], "brand_name": "Prednisolone Sodium Phosphate", "product_id": "69238-2122_c2b9ec45-c2e4-4b1e-897e-2ed95618d56e", "dosage_form": "SOLUTION", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "69238-2122", "generic_name": "Prednisolone Sodium Phosphate", "labeler_name": "Amneal Pharmaceuticals NY LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Prednisolone Sodium Phosphate", "active_ingredients": [{"name": "PREDNISOLONE SODIUM PHOSPHATE", "strength": "15 mg/5mL"}], "application_number": "ANDA216715", "marketing_category": "ANDA", "marketing_start_date": "20221027", "listing_expiration_date": "20261231"}