Acyclovir

Product NDC
68071-4528
11-digit product format
680714528
Labeler code
68071
Product ID
68071-4528_bd9a3eba-02c2-bb2f-e053-2995a90a51b0
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Acyclovir
Dosage form
CAPSULE
Route
ORAL
Labeler
NuCare Pharmaceuticals,Inc.
Application
ANDA201445
Marketing category
ANDA
Marketing start
2016-10-15
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
2022-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
68071-4528-36807145280330 CAPSULE in 1 BOTTLE (68071-4528-3) 30 capsule2018-08-150000-00-00NoNoCurrent
68071-4528-46807145280440 CAPSULE in 1 BOTTLE (68071-4528-4) 40 capsule2018-08-150000-00-00NoNoCurrent
68071-4528-66807145280660 CAPSULE in 1 BOTTLE (68071-4528-6) 60 capsule2018-08-150000-00-00NoNoCurrent