Methylprednisolone Acetate

Product NDC
0781-3131
11-digit product format
007813131
Labeler code
0781
Product ID
0781-3131_7b4e3280-2181-4cde-a5fa-e0caf53417a0
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Methylprednisolone Acetate
Dosage form
INJECTION, SUSPENSION
Route
INTRA-ARTICULAR; INTRALESIONAL; INTRAMUSCULAR; PARENTERAL; SOFT TISSUE
Labeler
Sandoz Inc
Application
ANDA040794
Marketing category
ANDA
Marketing start
2009-03-05
Marketing end
0000-00-00
Substance
METHYLPREDNISOLONE ACETATE
Active strength
40 mg/mL
Pharmacologic classes
Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
NDC exclude flag
E
Listing certified through
2018-12-31
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
b3918abe-5cd1-b0ce-abd7-2dd6732cde26Product name520260128
e1637c7c-52c4-49a3-b36b-61be755aab29Product name420230717
9eb3e96d-a1d4-4de3-aa3d-a629eea44815Product name420220316

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0781-3131-71ML - Milliliter0781-31316dd13c01-39a1-436a-8af8-8ea5aae7354712012-07-24
0781-3131-95ML - Milliliter0781-3131dd60b1bb-4237-414e-98d9-ec80a9de057012012-07-24

DailyMed Socrata Ingredients#

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1358610methylPREDNISolone acetate 40 MG/ML Injectable SuspensionPSNfaf608f3-a13d-4969-b1a6-bb0bc1de2a8e1
1358617methylPREDNISolone acetate 80 MG/ML Injectable SuspensionPSNfaf608f3-a13d-4969-b1a6-bb0bc1de2a8e1
1358610methylprednisolone acetate 40 MG/ML Injectable SuspensionSCDfaf608f3-a13d-4969-b1a6-bb0bc1de2a8e1
1358617methylprednisolone acetate 80 MG/ML Injectable SuspensionSCDfaf608f3-a13d-4969-b1a6-bb0bc1de2a8e1