hydroquinone time release

Product NDC
24979-144
11-digit product format
249790144
Labeler code
24979
Product ID
24979-144_82175e2e-4bce-4028-8404-30451274d5e8
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
hydroquinone
Dosage form
CREAM
Route
TOPICAL
Labeler
TWi Pharmaceuticals, Inc.
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2017-06-16
Marketing end
0000-00-00
Substance
HYDROQUINONE
Active strength
40 mg/g
Pharmacologic classes
Melanin Synthesis Inhibitor [EPC],Melanin Synthesis Inhibitors [MoA],Depigmenting Activity [PE]
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
24979-144-292024-08-21C16284748780-1ba0f9c33-0dab-a910-e053-dadaa90a0b852f065106-33ad-45f7-a392-08814c8cfd68
24979-144-292021-01-29C16284748780-1ba0f9c33-0dab-a910-e053-dadaa90a0b852f065106-33ad-45f7-a392-08814c8cfd68

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
24979-144-29GM - Gram24979-144bbd360ef-bbd0-46f4-90f0-7014a2598eaa12017-11-06