hydroxyzine pamoate

Product NDC
55700-742
11-digit product format
557000742
Labeler code
55700
Product ID
55700-742_cbb4a17b-f45c-401b-8d71-0da4a16bff8a
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
hydroxyzine pamoate
Dosage form
CAPSULE
Route
ORAL
Labeler
Quality Care Products, LLC
Application
ANDA086183
Marketing category
ANDA
Marketing start
2019-04-11
Marketing end
0000-00-00
Substance
HYDROXYZINE PAMOATE
Active strength
50 mg/1
Pharmacologic classes
Antihistamine [EPC],Histamine Receptor Antagonists [MoA]
NDC exclude flag
No
Listing certified through
2022-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
55700-742-902025-01-14C16284748780-1f386c64a-3c74-0266-e053-dadaa90a7c1ae5cec8de-8212-43ea-8f09-3e5b40ad8804
55700-742-902023-01-30C16284748780-1f386c64a-3c74-0266-e053-dadaa90a7c1ae5cec8de-8212-43ea-8f09-3e5b40ad8804

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
55700-742-90EA - Each55700-7422961873d-f92a-4d9d-82ef-73ba0d37f75212019-05-02

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
55700-742-905570007429090 CAPSULE in 1 BOTTLE (55700-742-90) 90 capsule2019-04-110000-00-00NoNoCurrent