Abacavir Sulfate

Product NDC
60505-3583
11-digit product format
605053583
Labeler code
60505
Product ID
60505-3583_91461f24-41ef-15e2-5587-19e620f10604
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Abacavir Sulfate
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Apotex Corp
Application
ANDA201570
Marketing category
ANDA
Marketing start
2012-12-17
Marketing end
2020-12-31
Substance
ABACAVIR SULFATE
Active strength
300 mg/1
Pharmacologic classes
Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Nucleoside Analog [EXT],Nucleoside Reverse Transcriptase Inhibitors [MoA]
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
60505-3583-6EA - Each60505-35835679a6d8-d8ae-467f-b9ad-a8155242c6c112013-02-13