methylprednisolone acetate

Generic: methylprednisolone acetate

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

Drug Facts

Product Profile

Brand Name methylprednisolone acetate
Generic Name methylprednisolone acetate
Labeler a-s medication solutions
Dosage Form INJECTION, SUSPENSION
Routes
INTRA-ARTICULAR INTRALESIONAL INTRAMUSCULAR INTRASYNOVIAL SOFT TISSUE
Active Ingredients

methylprednisolone acetate 40 mg/mL

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-5894
Product ID 50090-5894_40739c05-2fb7-4641-a618-9fa5b940480d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA210043
Listing Expiration 2026-12-31
Marketing Start 2019-05-20

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500905894
Hyphenated Format 50090-5894

Supplemental Identifiers

RxCUI
1743779
UNII
43502P7F0P

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 ANDA210043 (source: ndc)
Routes
INTRA-ARTICULAR INTRALESIONAL INTRAMUSCULAR INTRASYNOVIAL SOFT TISSUE
source: ndc

Resolved Composition

Strengths
  • 40 mg/mL
source: ndc
Packaging
  • 1 VIAL, SINGLE-DOSE in 1 CARTON (50090-5894-0) / 1 mL in 1 VIAL, SINGLE-DOSE
source: ndc

Packages (1)

50090-5894-0 1 VIAL, SINGLE-DOSE in 1 CARTON (50090-5894-0) / 1 mL in 1 VIAL, SINGLE-DOSE

Ingredients (1)

methylprednisolone acetate (40 mg/mL)

Linked Drug Pages (1)

Methylprednisolone acetate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRA-ARTICULAR", "INTRALESIONAL", "INTRAMUSCULAR", "INTRASYNOVIAL", "SOFT TISSUE"], "spl_id": "40739c05-2fb7-4641-a618-9fa5b940480d", "openfda": {"unii": ["43502P7F0P"], "rxcui": ["1743779"], "spl_set_id": ["1084208f-3b86-4aef-8247-5b6ed6cd50c7"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (50090-5894-0)  / 1 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "50090-5894-0", "marketing_start_date": "20220112"}], "brand_name": "Methylprednisolone acetate", "product_id": "50090-5894_40739c05-2fb7-4641-a618-9fa5b940480d", "dosage_form": "INJECTION, SUSPENSION", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "50090-5894", "generic_name": "Methylprednisolone acetate", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methylprednisolone acetate", "active_ingredients": [{"name": "METHYLPREDNISOLONE ACETATE", "strength": "40 mg/mL"}], "application_number": "ANDA210043", "marketing_category": "ANDA", "marketing_start_date": "20190520", "listing_expiration_date": "20261231"}