Valacyclovir Hydrochloride

Product NDC
85766-026
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Valacyclovir Hydrochloride
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Sportpharm LLC
Application
ANDA090682
Marketing category
ANDA
Substance
VALACYCLOVIR HYDROCHLORIDE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
85766-026-01100 TABLET, FILM COATED in 1 BOTTLE (85766-026-01) 2025-08-05NoHistorical
85766-026-022 TABLET, FILM COATED in 1 BOTTLE (85766-026-02) 2025-08-05NoHistorical
85766-026-044 TABLET, FILM COATED in 1 BOTTLE (85766-026-04) 2025-08-05NoHistorical
85766-026-05500 TABLET, FILM COATED in 1 BOTTLE (85766-026-05) 2025-08-05NoHistorical
85766-026-066 TABLET, FILM COATED in 1 BOTTLE (85766-026-06) 2025-09-24NoHistorical
85766-026-077 TABLET, FILM COATED in 1 BOTTLE (85766-026-07) 2025-08-05NoHistorical
85766-026-1010 TABLET, FILM COATED in 1 BOTTLE (85766-026-10) 2025-08-05NoHistorical
85766-026-1414 TABLET, FILM COATED in 1 BOTTLE (85766-026-14) 2025-08-05NoHistorical
85766-026-1515 TABLET, FILM COATED in 1 BOTTLE (85766-026-15) 2025-08-05NoHistorical
85766-026-2020 TABLET, FILM COATED in 1 BOTTLE (85766-026-20) 2025-08-05NoHistorical
85766-026-3030 TABLET, FILM COATED in 1 BOTTLE (85766-026-30) 2025-08-05NoHistorical
85766-026-551500 TABLET, FILM COATED in 1 BOTTLE (85766-026-55) 2025-08-05NoHistorical
85766-026-6060 TABLET, FILM COATED in 1 BOTTLE (85766-026-60) 2025-08-05NoHistorical
85766-026-9090 TABLET, FILM COATED in 1 BOTTLE (85766-026-90) 2025-08-05NoHistorical

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