VITRASE

Product NDC
24208-002
11-digit product format
242080002
Labeler code
24208
Product ID
24208-002_22bb835d-0433-4e75-bada-5cb60113d298
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
hyaluronidase, ovine
Dosage form
INJECTION, SOLUTION
Route
SUBCUTANEOUS
Labeler
Bausch & Lomb Incorporated
Application
BLA021640
Marketing category
BLA
Marketing start
2005-02-01
Marketing end
0000-00-00
Substance
HYALURONIDASE, OVINE
Active strength
200 [USP'U]/mL
Pharmacologic classes
Endoglycosidase [EPC],Glycoside Hydrolases [CS]
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
24208-002-01ML - Milliliter24208-0024d7349a6-456c-4aab-b64b-19105ba337df12013-05-02
24208-002-02ML - Milliliter24208-0024a0a1077-df82-4cf0-9ec4-1e403d72052512015-10-02

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
24208-002VITRASE (HYALURONIDASE, OVINE) INJECTION, SOLUTION [BAUSCH & LOMB INCORPORATED]8Legacy NDC20240530_21fbd12e-4a12-4ad1-ad01-964cd5ec9996.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
24208-002-02242080002022 VIAL, SINGLE-USE in 1 CARTON (24208-002-02) > 1.2 mL in 1 VIAL, SINGLE-USE2005-02-010000-00-00NoNoCurrent