FDA.reportPublic FDA data

Verapamil Hydrochloride

Product NDC
0093-3044
11-digit product format
000933044
Labeler code
0093
Product ID
0093-3044_dfa87de0-b5a5-45d8-af05-76bcb35e2123
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
verapamil hydrochloride
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Labeler
Teva Pharmaceuticals USA Inc
Application
ANDA074587
Marketing category
ANDA
Marketing start
2014-01-29
Marketing end
2020-01-31
Substance
VERAPAMIL HYDROCHLORIDE
Active strength
180 mg/1
Pharmacologic classes
P-Glycoprotein Inhibitors [MoA],Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC],Cytochrome P450 3A4 Inhibitors [MoA],Cytochrome P450 3A Inhibitors [MoA]
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
ea1f6fc8-bfc2-4421-a2eb-4e87c7c3e3c4Product name220230103
33ad674d-d105-6aa5-02fa-95ae4329b8cdProduct name220180809
3279bd6d-5b02-e60b-3857-c853a2deb2ddProduct name220170713
8ebb66e3-d7b3-f1e5-88aa-3369e64bb84aProduct name120140508
940a1faa-2df8-cc65-be37-1b97984b4ea3Product name120140508
d3b67bc2-0e96-e3ec-06a9-90afcc07bf13Product name120140508
e2fcd66c-a043-3187-790d-b0342deb1149Product name120140508

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0093-3044-01EA - Each0093-3044744d3b8b-f902-491f-b970-4be051519b0a12014-02-04
0093-3044-05EA - Each0093-3044e8374d0b-5ccb-40af-baa4-f8b74c011e9312014-06-03

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
897640verapamil HCl 180 MG Extended Release Oral TabletPSN34ebe927-ef58-4799-8a9e-3e8a8d6f47282
897640verapamil hydrochloride 180 MG Extended Release Oral TabletSCD34ebe927-ef58-4799-8a9e-3e8a8d6f47282