Gentak

Product NDC
49999-159
11-digit product format
499990159
Labeler code
49999
Product ID
49999-159_a0e3b94b-4eac-40ab-9895-e0cf62a866e1
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Gentamicin Sulfate
Dosage form
OINTMENT
Route
OPHTHALMIC
Labeler
Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Application
ANDA064093
Marketing category
ANDA
Marketing start
2012-03-27
Marketing end
0000-00-00
Substance
GENTAMICIN SULFATE
Active strength
3 mg/g
Pharmacologic classes
Aminoglycoside Antibacterial [EPC],Aminoglycosides [CS]
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
49999-159-35GM - Gram49999-15995c53254-0508-4442-b1c1-b3b82938e53612012-07-24