ReadySharp Dexamethasone

Product NDC
68788-7441
11-digit product format
687887441
Labeler code
68788
Product ID
68788-7441_d02cf799-769f-45b0-82fd-c5ea03385fa7
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Dexamethasone Sodium Phosphate
Dosage form
INJECTION
Route
INTRAMUSCULAR; INTRAVENOUS
Labeler
Preferred Pharmaceuticals, Inc.
Application
ANDA087702
Marketing category
ANDA
Marketing start
1982-09-07
Marketing end
0000-00-00
Substance
DEXAMETHASONE SODIUM PHOSPHATE
Active strength
10 mg/mL
Pharmacologic classes
Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
68788-7441-1EA - Each68788-74419b64a0b1-9861-4a38-b02d-34b28995ada512020-04-20