Acyclovir

Product NDC
63187-182
11-digit product format
631870182
Labeler code
63187
Product ID
63187-182_347e3045-6810-4821-ab70-0ba268a4cc2e
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Acyclovir
Dosage form
CAPSULE
Route
ORAL
Labeler
Proficient Rx LP
Application
ANDA075090
Marketing category
ANDA
Marketing start
2009-10-22
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

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
63187-182ACYCLOVIR CAPSULE [PROFICIENT RX LP]3Legacy NDC20210121_b2c19660-4f9e-48e2-9918-5954962c45ab.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
63187-182-306318701823030 CAPSULE in 1 BOTTLE, PLASTIC (63187-182-30) 30 capsule2019-01-010000-00-00NoNoCurrent
63187-182-606318701826060 CAPSULE in 1 BOTTLE, PLASTIC (63187-182-60) 60 capsule2019-01-010000-00-00NoNoCurrent
63187-182-906318701829090 CAPSULE in 1 BOTTLE, PLASTIC (63187-182-90) 90 capsule2019-01-010000-00-00NoNoCurrent