Hyaluronic Acid

Product NDC
77651-4162
11-digit product format
776514162
Labeler code
77651
Product ID
77651-4162_a75e2bb2-f89b-53f4-e053-2a95a90a93c7
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Hyaluronic Acid
Dosage form
INJECTION
Route
INTRAEPIDERMAL
Labeler
Quimfa S.A
Application
ANDA076559
Marketing category
ANDA
Marketing start
2002-12-06
Marketing end
0000-00-00
Substance
HYALURONIC ACID
Active strength
3 g/1
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
77651-4162-62022-01-28C16284748780-1d6a99b39-c2a3-a426-e053-dadaa90af4c2a75e2bb2-f89a-53f4-e053-2a95a90a93c7

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
77651-4162-6Hyaluronic Acid1 in 1 SYRINGEINJECTION11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
77651-4162HYALURONIC ACID INJECTION [QUIMFA S.A]1Legacy NDC, 1 package rows20200616_a75e2bb2-f89a-53f4-e053-2a95a90a93c7.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionStatus
77651-4162-6776514162061 in 1 SYRINGEHistorical