hydroxyzine pamoate

Product NDC
50090-2664
11-digit product format
500902664
Labeler code
50090
Product ID
50090-2664_3ad664f2-f64e-49f8-9669-85eff6afabc4
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
hydroxyzine pamoate
Dosage form
CAPSULE
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA086183
Marketing category
ANDA
Marketing start
1981-12-14
Marketing end
0000-00-00
Substance
HYDROXYZINE PAMOATE
Active strength
50 mg/1
Pharmacologic classes
Antihistamine [EPC],Histamine Receptor Antagonists [MoA]
NDC exclude flag
E
Listing certified through
2018-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
50090-2664-02020-01-31C16284748780-19d75b9cf-d1ea-f424-e053-dadaa90a57ce6f7dc4d2-5986-435c-aa2b-ef8586e56029

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
50090-2664-0EA - Each50090-266452ee25eb-2b4e-4ceb-957d-97f4ce5ac96812019-04-11