Dexamethasone Sodium Phosphate

Product NDC
70518-0872
11-digit product format
705180872
Labeler code
70518
Product ID
70518-0872_5f11c756-56a0-5c29-e053-2a91aa0a723c
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
DEXAMETHASONE SODIUM PHOSPHATE
Dosage form
INJECTION, SOLUTION
Route
INTRAMUSCULAR; INTRAVENOUS
Labeler
REMEDYREPACK INC.
Application
ANDA084916
Marketing category
ANDA
Marketing start
2017-11-28
Marketing end
0000-00-00
Substance
DEXAMETHASONE SODIUM PHOSPHATE
Active strength
4 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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70518-0872-02020-05-07C16284748780-19d75b9d0-f388-f424-e053-dadaa90a57ced7ef24a8-a5a4-4e21-98f2-4ebcbce94edc
70518-0872-02020-01-31C16284748780-19d75b9d0-f388-f424-e053-dadaa90a57ced7ef24a8-a5a4-4e21-98f2-4ebcbce94edc