valacyclovir hydrochloride

Generic: valacyclovir hydrochloride

Labeler: jubilant cadista pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name valacyclovir hydrochloride
Generic Name valacyclovir hydrochloride
Labeler jubilant cadista pharmaceuticals inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

valacyclovir hydrochloride 500 mg/1

Manufacturer
Jubilant Cadista Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 59746-324
Product ID 59746-324_40211dd2-c21e-45a4-a8d4-04febf925f52
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA201506
Listing Expiration 2026-12-31
Marketing Start 2012-04-05

Pharmacologic Class

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]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 59746324
Hyphenated Format 59746-324

Supplemental Identifiers

RxCUI
313564 313565
UNII
G447S0T1VC

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name valacyclovir hydrochloride (source: ndc)
Generic Name valacyclovir hydrochloride (source: ndc)
Application Number ANDA201506 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (59746-324-01)
  • 10 TABLET, FILM COATED in 1 BOTTLE (59746-324-10)
  • 30 TABLET, FILM COATED in 1 BOTTLE (59746-324-30)
  • 250 TABLET, FILM COATED in 1 BOTTLE (59746-324-37)
  • 300 TABLET, FILM COATED in 1 BOTTLE (59746-324-47)
  • 90 TABLET, FILM COATED in 1 BOTTLE (59746-324-90)
source: ndc

Packages (6)

Ingredients (1)

valacyclovir hydrochloride (500 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "40211dd2-c21e-45a4-a8d4-04febf925f52", "openfda": {"unii": ["G447S0T1VC"], "rxcui": ["313564", "313565"], "spl_set_id": ["3277c17e-f953-2b0a-fe0a-4f5d1aeace9d"], "manufacturer_name": ["Jubilant Cadista Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (59746-324-01)", "package_ndc": "59746-324-01", "marketing_start_date": "20120405"}, {"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE (59746-324-10)", "package_ndc": "59746-324-10", "marketing_start_date": "20120405"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (59746-324-30)", "package_ndc": "59746-324-30", "marketing_start_date": "20120405"}, {"sample": false, "description": "250 TABLET, FILM COATED in 1 BOTTLE (59746-324-37)", "package_ndc": "59746-324-37", "marketing_start_date": "20120405"}, {"sample": false, "description": "300 TABLET, FILM COATED in 1 BOTTLE (59746-324-47)", "package_ndc": "59746-324-47", "marketing_start_date": "20120405"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (59746-324-90)", "package_ndc": "59746-324-90", "marketing_start_date": "20120405"}], "brand_name": "valacyclovir hydrochloride", "product_id": "59746-324_40211dd2-c21e-45a4-a8d4-04febf925f52", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["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]"], "product_ndc": "59746-324", "generic_name": "valacyclovir hydrochloride", "labeler_name": "Jubilant Cadista Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "valacyclovir hydrochloride", "active_ingredients": [{"name": "VALACYCLOVIR HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA201506", "marketing_category": "ANDA", "marketing_start_date": "20120405", "listing_expiration_date": "20261231"}