FDA.reportPublic FDA data

acyclovir

Product NDC
49999-231
11-digit product format
499990231
Labeler code
49999
Product ID
49999-231_2d7da70d-220e-4bb6-a8c5-c6f9438dd91d
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
acyclovir
Dosage form
TABLET
Route
ORAL
Labeler
Lake Erie Medical DBA Quality Care Products LLC
Application
ANDA077309
Marketing category
ANDA
Marketing start
2006-03-13
Marketing end
0000-00-00
Substance
ACYCLOVIR
Active strength
800 mg/1
Pharmacologic classes
DNA Polymerase Inhibitors [MoA],Herpes Simplex Virus Nucleoside Analog DNA Polymerase Inhibitor [EPC],Herpes Zoster Virus Nucleoside Analog DNA Polymerase Inhibitor [EPC],Herpesvirus Nucleoside Analog DNA Polymerase Inhibitor [EPC],Nucleoside Analog [EXT]
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
49999-231-00EA - Each49999-231f8ae434d-737c-43e1-a93b-3cac5b7cd42f12015-04-03
49999-231-15EA - Each49999-231549addac-72fd-455a-bed8-21ab729a2efe12015-04-03
49999-231-30EA - Each49999-231be579cc1-6f9b-4b1d-8936-1961ee7c7d5612015-04-03
49999-231-35EA - Each49999-23160cbf43f-343d-4f9f-b82e-40a8433b50bb12015-04-03
49999-231-40EA - Each49999-2319f9233aa-415d-46c0-b695-6e7aba1bb6a312017-03-06