methylprednisolone acetate
Generic: methylprednisolone acetate
Labeler: sandoz inc.Drug Facts
Product Profile
Brand Name
methylprednisolone acetate
Generic Name
methylprednisolone acetate
Labeler
sandoz inc.
Dosage Form
INJECTION, SUSPENSION
Routes
Active Ingredients
methylprednisolone acetate 80 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
0781-3516
Product ID
0781-3516_ab8910e5-0b8c-4057-a95d-4519ce85835b
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA214870
Listing Expiration
2026-12-31
Marketing Start
2023-02-08
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
07813516
Hyphenated Format
0781-3516
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
methylprednisolone acetate (source: ndc)
Generic Name
methylprednisolone acetate (source: ndc)
Application Number
ANDA214870 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 80 mg/mL
Packaging
- 1 VIAL, MULTI-DOSE in 1 CARTON (0781-3516-75) / 5 mL in 1 VIAL, MULTI-DOSE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRALESIONAL", "INTRAMUSCULAR", "INTRASYNOVIAL", "SOFT TISSUE"], "spl_id": "ab8910e5-0b8c-4057-a95d-4519ce85835b", "openfda": {"unii": ["43502P7F0P"], "rxcui": ["1358610", "1358617"], "spl_set_id": ["a363f0cd-9c8e-4622-9271-171706846b96"], "manufacturer_name": ["Sandoz Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, MULTI-DOSE in 1 CARTON (0781-3516-75) / 5 mL in 1 VIAL, MULTI-DOSE", "package_ndc": "0781-3516-75", "marketing_start_date": "20230208"}], "brand_name": "METHYLPREDNISOLONE ACETATE", "product_id": "0781-3516_ab8910e5-0b8c-4057-a95d-4519ce85835b", "dosage_form": "INJECTION, SUSPENSION", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "0781-3516", "generic_name": "METHYLPREDNISOLONE ACETATE", "labeler_name": "Sandoz Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "METHYLPREDNISOLONE ACETATE", "active_ingredients": [{"name": "METHYLPREDNISOLONE ACETATE", "strength": "80 mg/mL"}], "application_number": "ANDA214870", "marketing_category": "ANDA", "marketing_start_date": "20230208", "listing_expiration_date": "20261231"}