Moexipril Hydrochloride

Product NDC
68151-1472
11-digit product format
681511472
Labeler code
68151
Product ID
68151-1472_2517e55f-cae7-4b4a-8565-7f3569a66ca7
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Moexipril Hydrochloride
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Carilion Materials Management
Application
ANDA076204
Marketing category
ANDA
Marketing start
2003-05-08
Marketing end
0000-00-00
Substance
MOEXIPRIL HYDROCHLORIDE
Active strength
8 mg/1
Pharmacologic classes
Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA]
NDC exclude flag
E
Listing certified through
2018-12-31
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
fb7ab793-2c12-4079-b100-a64f73bef25aProduct name420240712
b0cbf770-6cc3-4aa4-9158-755110c2b9f7Product name220230717
dc7c5daa-021f-40dd-b00d-63982cb2067aProduct name120230426
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name520200925
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
419aab54-5d5a-4146-9453-026d4a9991beProduct name220170525
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name220160823
89dac932-b90a-4410-9ab1-84c53e57de25Product name120150316
041df61b-f8b6-48a6-7b67-411e1412678bProduct name120140508
af9cc3a2-6f01-38ca-6e6b-5199b2c3eeecProduct name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
68151-1472-02020-01-31C16284748780-19d75b9d1-1e33-f424-e053-dadaa90a57ceMOEXIPRIL HYDROCHLORIDE TABLETS USP, 7.5 mg and 15 mg 0017 5150 Rx only

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68151-1472-0Moexipril Hydrochloride1 in 1 PACKAGETABLET, FILM COATED15

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
MOEXIPRIL HYDROCHLORIDEACTIVE INGREDIENTQ1UMG3UH45MOEXIPRIL HYDROCHLORIDE TABLET, FILM COATED [CARILION MATERIALS MANAGEMENT]2
MOEXIPRILATACTIVE MOIETYH3753190JSMOEXIPRIL HYDROCHLORIDE TABLET, FILM COATED [CARILION MATERIALS MANAGEMENT]2
CROSPOVIDONEINACTIVE INGREDIENT68401960MKMOEXIPRIL HYDROCHLORIDE TABLET, FILM COATED [CARILION MATERIALS MANAGEMENT]2
FERRIC OXIDE REDINACTIVE INGREDIENT1K09F3G675MOEXIPRIL HYDROCHLORIDE TABLET, FILM COATED [CARILION MATERIALS MANAGEMENT]2
HYPROMELLOSE 2910 (15 MPA.S)INACTIVE INGREDIENT36SFW2JZ0WMOEXIPRIL HYDROCHLORIDE TABLET, FILM COATED [CARILION MATERIALS MANAGEMENT]2
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENT0VUT3PMY82MOEXIPRIL HYDROCHLORIDE TABLET, FILM COATED [CARILION MATERIALS MANAGEMENT]2
LACTOSE MONOHYDRATEINACTIVE INGREDIENTEWQ57Q8I5XMOEXIPRIL HYDROCHLORIDE TABLET, FILM COATED [CARILION MATERIALS MANAGEMENT]2
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I30MOEXIPRIL HYDROCHLORIDE TABLET, FILM COATED [CARILION MATERIALS MANAGEMENT]2
SODIUM BICARBONATEINACTIVE INGREDIENT8MDF5V39QOMOEXIPRIL HYDROCHLORIDE TABLET, FILM COATED [CARILION MATERIALS MANAGEMENT]2
STARCH, CORNINACTIVE INGREDIENTO8232NY3SJMOEXIPRIL HYDROCHLORIDE TABLET, FILM COATED [CARILION MATERIALS MANAGEMENT]2
TITANIUM DIOXIDEINACTIVE INGREDIENT15FIX9V2JPMOEXIPRIL HYDROCHLORIDE TABLET, FILM COATED [CARILION MATERIALS MANAGEMENT]2
TRIACETININACTIVE INGREDIENTXHX3C3X673MOEXIPRIL HYDROCHLORIDE TABLET, FILM COATED [CARILION MATERIALS MANAGEMENT]2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68151-1472MOEXIPRIL HYDROCHLORIDE TABLET, FILM COATED [CARILION MATERIALS MANAGEMENT]5Legacy NDC, 1 package rows20171227_83a79dc8-3c0d-434f-b7ed-13af9f340994.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1299896moexipril HCl 15 MG Oral TabletPSN83a79dc8-3c0d-434f-b7ed-13af9f3409945
1299897moexipril HCl 7.5 MG Oral TabletPSN83a79dc8-3c0d-434f-b7ed-13af9f3409945
1299896moexipril hydrochloride 15 MG Oral TabletSCD83a79dc8-3c0d-434f-b7ed-13af9f3409945
1299897moexipril hydrochloride 7.5 MG Oral TabletSCD83a79dc8-3c0d-434f-b7ed-13af9f3409945

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionStatus
68151-1472-0681511472001 in 1 PACKAGEHistorical