Acyclovir

Product NDC
43063-701
11-digit product format
430630701
Labeler code
43063
Product ID
43063-701_7cd6f80a-f47e-2088-e053-2991aa0a7ffc
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Acyclovir
Dosage form
CAPSULE
Route
ORAL
Labeler
PD-Rx Pharmaceuticals, Inc.
Application
ANDA075090
Marketing category
ANDA
Marketing start
2015-02-01
Marketing end
0000-00-00
Substance
ACYCLOVIR
Active strength
200 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
43063-701-35EA - Each43063-7018736982e-b422-408e-955e-559a0661f63812016-09-02
43063-701-50EA - Each43063-701ab6fe42a-751d-419b-9a94-0ef14a5fbb5912016-09-02