Betamethasone Sodium Phosphate and Betamethasone Acetate

Product NDC
40042-048
11-digit product format
400420048
Labeler code
40042
Product ID
40042-048_f8cfe50b-e269-47f2-8ce6-0b40511945bc
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Betamethasone Sodium Phosphate and Betamethasone Acetate
Dosage form
INJECTION, SUSPENSION
Route
INTRA-ARTICULAR; INTRALESIONAL; INTRAMUSCULAR
Labeler
PharmaForce, Inc.
Application
ANDA090747
Marketing category
ANDA
Marketing start
2009-07-31
Marketing end
0000-00-00
Substance
BETAMETHASONE ACETATE; BETAMETHASONE SODIUM PHOSPHATE
Active strength
3 mg/mL; mg/mL
Pharmacologic classes
Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA],Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
40042-048-052019-10-21C16284748780-1956f9ecf-d4d9-621f-e053-dbdaa90a74adfe8f2272-294b-451d-95f5-7ea1642e949e