Home NDC 63187-182 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 NDC Dashboard title SPL version Validation Dashboard ZIP 63187-182 ACYCLOVIR CAPSULE [PROFICIENT RX LP] 3 Legacy NDC 20210121_b2c19660-4f9e-48e2-9918-5954962c45ab.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 63187-182-30 63187018230 30 CAPSULE in 1 BOTTLE, PLASTIC (63187-182-30) 30 capsule 2019-01-01 0000-00-00 No No Current 63187-182-60 63187018260 60 CAPSULE in 1 BOTTLE, PLASTIC (63187-182-60) 60 capsule 2019-01-01 0000-00-00 No No Current 63187-182-90 63187018290 90 CAPSULE in 1 BOTTLE, PLASTIC (63187-182-90) 90 capsule 2019-01-01 0000-00-00 No No Current