HYPROMELLOSE 2910 (3 MPA.S)

Substance profile for UNII 0VUT3PMY82, enriched with FDA NDC listings, DailyMed labels, legacy aliases, and open chemistry identifiers.

Substance Identity#

UNII
0VUT3PMY82
Preferred term
HYPROMELLOSE 2910 (3 MPA.S)
Registry number
9004-65-3
Ingredient type
INGREDIENT SUBSTANCE
Molecular formula
Polymer substance not supported

Chemical And Database Identifiers#

RxCUI
1300449
PubChem
0
NCIt
C82311
INN ID
0

Open Chemistry Sources#

DailyMed Socrata Ingredients#

Ingredient, Type, DailyMed label table
IngredientTypeDailyMed labelSPL version
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTETODOLAC3
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTLEVETIRACETAM3
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTThese highlights do not include all the information needed to use topiramate tablets, USP safely and effectively. See full prescribing information for topiramate tablets, USPTopiramate Tablets, USP for oral use Initial U.S. Approval: 19965
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTALPRAZOLAM1
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTTOPIRAMATE1
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTTOPIRAMATE6
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTNABUMETONE2
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTInflamation Reduction Pack2
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTTriamterene and Hydrochlorothiazide Tablets, USP2
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTLEVOFLOXACIN3
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTTemazepam Capsules, USP CIV1
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTGemfibrozil Tablets, USP 600 mg3
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTCitalopram Tablets, USP Rx Only4
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTMETOPROLOL TARTRATE TABLETS USP 0733 07341
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTTriamterene and Hydrochlorothiazide Tablets, USP1
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTSertraline Tablets, USP 25 mg, 50 mg and 100 mg Rx Only27
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTThese highlights do not include all the information needed to use pantoprazole sodium delayed-release tablets safely and effectively. See full prescribing information for pantoprazole sodium delayed-release tablets. PANTOPRAZOLE sodium delayed-release tablets USP, for oral administration Initial U.S. approval: 20002
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTThese highlights do not include all the information needed to use levetiracetam tablets safely and effectively. See full prescribing information for levetiracetam tablets USP. Levetiracetam Tablets USP for Oral Use Initial U.S. Approval: 19992
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTThese highlights do not include all the information needed to use raloxifene hydrochloride tablets, USP safely and effectively. See full prescribing information for raloxifene hydrochloride tablets, USP. Raloxifene Hydrochloride Tablets, USP for Oral Use Initial U.S. Approval: 19971
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTThese highlights do not include all the information needed to use duloxetine delayed-release capsules USP safely and effectively. See full prescribing information for duloxetine delayed-release capsules USP. DULOXETINE delayed-release capsules USP for oral use Initial U.S. Approval: 20042
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTRevised: August 2014 Mirtazapine Tablets, USP Rx only2
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTDesipramine Hydrochloride Tablets, USP1001
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTThese highlights do not include all the information needed to use divalproex sodium extended-release tablets USP safely and effectively. See full prescribing information for divalproex sodium extended-release tablets USP. DIVALPROEX Sodium Extended-Release Tablets USP, for Oral Use Initial U.S. Approval: 20002
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTThese highlights do not include all the information needed to use TRICOR safely and effectively. See full prescribing information for TRICOR. TRICOR (fenofibrate) Tablet for oral use Initial U.S. Approval: 19932
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTThese highlights do not include all the information needed to use levetiracetam tablets safely and effectively. See full prescribing information for levetiracetam tablets. LEVETIRACETAM Tablets USP, for oral use Initial U.S. Approval: 19992
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTThese highlights do not include all the information needed to use metoprolol succinate extended-release tablets USP safely and effectively. See full prescribing information for metoprolol succinate extended release tablets USP. Metoprolol succinate extended-release tablets USP Initial U.S. Approval: 19921
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTThese highlights do not include all the information needed to use quetiapine fumarate tablets safely and effectively. See full prescribing information for quetiapine fumarate tablets. QUETIAPINE fumarate tablets for oral use Initial U.S. Approval: 19972
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTSertraline Hydrochloride Tablets 25 mg, 50 mg and 100 mg1
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTTopiramate Tablets1
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTMirtazapine Tablets USP Revised: June 2012 Rx only1
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTThese highlights do not include all the information needed to use levetiracetam tablets safely and effectively. See full prescribing information for levetiracetam tablets. Levetiracetam Tablets USP, for oral use Initial U.S. Approval: 19991
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTFluvoxamine Maleate Tablets These highlights do not include all the information needed to use Fluvoxamine Maleate Tablets safely and effectively. See full prescribing information for Fluvoxamine Maleate Tablets. Fluvoxamine Maleate Tablets for oral administration Initial U.S. Approval: 19941
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTFENOFIBRATE TABLETS, 54 mg and 160 mg1
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTMETOPROLOL TARTRATE TABLETS USP1
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTFluphenazine Hydrochloride Tablets, USP14
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTFluphenazine Hydrochloride Tablets, USP2
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTThese highlights do not include all the information needed to use levetiracetam tablets safely and effectively. See full prescribing information for levetiracetam tablets USP. Levetiracetam Tablets USP for Oral Use Initial U.S. Approval: 19991
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTCYCLOBENZAPRINE HYDROCHLORIDE TABLETS USP1
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTLevetiracetam Tablets Rx Only Revised: March, 20113
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTTemazepam Capsules, USP CIV2
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTMETOPROLOL TARTRATE TABLETS USP 0733 07341
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTHIGHLIGHTS OF PRESCRIBING INFORMATION These highlights do not include all the information needed to use Amoxicillin and Clavulanate Potassium Tablets USP, Amoxicillin and Clavulanate Potassium for Oral Suspension USP, and Amoxicillin and Clavulanate Potassium Tablets USP (Chewable) safely and effectively. See full prescribing information for Amoxicillin and Clavulanate Potassium Tablets USP, Amoxicillin and Clavulanate Potassium for Oral Suspension USP, and Amoxicillin and Clavulanate Potassium Tablets USP1
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTThese highlights do not include all the information needed to use fluoxetine capsules USP safely and effectively. See full prescribing information for fluoxetine capsules USP. FLUOXETINE capsules USP for oral use Initial U.S. Approval: 1987x1
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTPAROXETINE TABLETS USP, 10 mg, 20 mg, 30 mg and 40 mg 7114 7115 7116 7121 Rx only1
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTSertraline Hydrochloride Tablets 25 mg, 50 mg and 100 mg4
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTSertraline Hydrochloride Tablets 25 mg, 50 mg and 100 mg2
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTThese highlights do not include all the information needed to use levofloxacin tablets safely and effectively. See full prescribing information for levofloxacin tablets. LEVOFLOXACIN tablets for oral use Initial U.S. Approval: 1996 To reduce the development of drug-resistant bacteria and maintain the effectiveness of levofloxacin and other antibacterial drugs, levofloxacin should be used only to treat or prevent infections that are proven or strongly suspected to be caused by bacteria.1000
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTThese highlights do not include all the information needed to use carvedilol tablets USP safely and effectively. See full prescribing information for carvedilol tablets USP. CARVEDILOL tablets USP for oral use Initial U.S. Approval: 19951
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTTriamterene and Hydrochlorothiazide Tablets, USP2
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTThese highlights do not include all the information needed to use metoprolol succinate extended-release tablets USP safely and effectively. See full prescribing information for metoprolol succinate extended release tablets USP. Metoprolol succinate extended-release tablets USP Initial U.S. Approval: 19923
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTMirtazapine Tablets USP Revised: June 2012 Rx only1
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTAMOXICILLIN AND CLAVULANATE POTASSIUM TABLETS USP, 500 mg/125 mg and 875 mg/125 mg 2274 2275 Rx only1
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTThese highlights do not include all the information needed to use AVANDAMET safely and effectively. See full prescribing information for AVANDAMET. AVANDAMET (rosiglitazone maleate and metformin hydrochloride) Tablets Initial U.S. Approval: 20026
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENT4aad770b-a342-45c5-8199-21a1240603141
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTMirtazapine Tablets USP Revised: June 2008 Rx only1
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTThese highlights do not include all the information needed to use lamivudine and zidovudine tablets USP safely and effectively. See full prescribing information for lamivudine and zidovudine tablets USP. LAMIVUDINE and ZIDOVUDINE tablets, USP 150 mg/300 mg for oral use Initial U.S. Approval: 19971
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTDrug Facts1
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTThese highlights do not include all the information needed to use levofloxacin tablets safely and effectively. See full prescribing information for levofloxacin tablets. LEVOFLOXACIN tablets for oral use Initial U.S. Approval: 1996 To reduce the development of drug-resistant bacteria and maintain the effectiveness of levofloxacin and other antibacterial drugs, levofloxacin should be used only to treat or prevent infections that are proven or strongly suspected to be caused by bacteria.1
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTDrug Facts2
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTThese highlights do not include all the information needed to use lamivudine and zidovudine tablets USP safely and effectively. See full prescribing information for lamivudine and zidovudine tablets USP. LAMIVUDINE and ZIDOVUDINE tablets, USP 150 mg/300 mg for oral use Initial U.S. Approval: 19971
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTAMOXICILLIN AND CLAVULANATE POTASSIUM TABLETS USP, 500 mg/125 mg and 875 mg/125 mg 2274 2275 Rx only1
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTTriamterene and Hydrochlorothiazide Tablets, USP2
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTClarithromycin Tablets, USP3
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTLevetiracetam1
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTMirtazapine Tablets USP Revised: June 2008 Rx only1
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTCitalopram Tablets, USP1
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTAMOXICILLIN AND CLAVULANATE POTASSIUM TABLETS USP, 500 mg/125 mg and 875 mg/125 mg 2274 2275 Rx only1
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTTemazepam Capsules, USP CIV2
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTSertraline Hydrochloride Tablets 25 mg, 50 mg and 100 mg1
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTThese highlights do not include all the information needed to use carvedilol tablets USP safely and effectively. See full prescribing information for carvedilol tablets USP. CARVEDILOL tablets USP for oral use Initial U.S. Approval: 19951
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTThese highlights do not include all the information needed to use metoprolol succinate extended-release tablets USP safely and effectively. See full prescribing information for metoprolol succinate extended release tablets USP. Metoprolol succinate extended-release tablets USP Initial U.S. Approval: 19921
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTThese highlights do not include all the information needed to use levofloxacin tablets safely and effectively. See full prescribing information for levofloxacin tablets. LEVOFLOXACIN tablets for oral use Initial U.S. Approval: 1996 To reduce the development of drug-resistant bacteria and maintain the effectiveness of levofloxacin and other antibacterial drugs, levofloxacin should be used only to treat or prevent infections that are proven or strongly suspected to be caused by bacteria.1
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTThese highlights do not include all the information needed to use levofloxacin tablets safely and effectively. See full prescribing information for levofloxacin tablets. LEVOFLOXACIN tablets for oral use Initial U.S. Approval: 1996 To reduce the development of drug-resistant bacteria and maintain the effectiveness of levofloxacin and other antibacterial drugs, levofloxacin should be used only to treat or prevent infections that are proven or strongly suspected to be caused by bacteria.3
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTSertraline Hydrochloride Tablets 25 mg, 50 mg and 100 mg1
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTThese highlights do not include all the information needed to use metoprolol succinate extended-release tablets USP safely and effectively. See full prescribing information for metoprolol succinate extended release tablets USP. Metoprolol succinate extended-release tablets USP for Oral Use Initial U.S. Approval: 19923
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTLorazepam Tablets, USP6
HYPROMELLOSE 2910 (3 MPA.S)ACTIVE INGREDIENTNature's Tears Drug Facts1
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTDesipramine Hydrochloride Tablets, USP1
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTTramadol Hydrochloride and Acetaminophen Tablets 37.5 mg/325 mg1
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTHYDROCODONE BITARTRATE AND IBUPROFEN TABLETS 7.5 mg/200 mg1
HYPROMELLOSE 2910 (3 CPS)INACTIVE INGREDIENTTramadol Hydrochloride and Acetaminophen Tablets 37.5 mg/325 mg2
HYPROMELLOSE 2910 (3 CPS)INACTIVE INGREDIENTDesipramine Hydrochloride Tablets, USP1
HYPROMELLOSE 2910 (3 CPS)INACTIVE INGREDIENTRanitidine Tablets, USP and Ranitidine Capsules1
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTFENOFIBRATE TABLETS, 54 mg and 160 mg2
HYPROMELLOSE 2910 (3 CPS)INACTIVE INGREDIENT71d80d65-592d-4eec-84ba-d6f97c1351611
hypromellose 2910 (3 cps)INACTIVE INGREDIENTThese highlights do not include all the information needed to use Ranexa safely and effectively. See full prescribing information for Ranexa. Ranexa (ranolazine) extended-release tablets Initial U.S. Approval: 20062
HYPROMELLOSE 2910 (3 CPS)INACTIVE INGREDIENTRanitidine Tablets, USP and Ranitidine Capsules1
HYPROMELLOSE 2910 (3 CPS)INACTIVE INGREDIENTef14122b-7fff-45fa-b13b-0ea9e48bd57d1
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTMethazolamide Tablets, USP1
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTCITALOPRAM TABLET [LAKE ERIE MEDICAL & SURGICAL SUPPLY DBA QUALITY CARE PRODUCTS LLC]3973
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTHYDROCODONE BITARTRATE AND IBUPROFEN TABLET, FILM COATED [LAKE ERIE MEDICAL DBA QUALITY CARE PRODUCTS LLC]3325
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTTRICOR (FENOFIBRATE) TABLET [ABBVIE INC.]1426
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTLEVETIRACETAM TABLET, FILM COATED [BRYANT RANCH PREPACK]1001
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTNALTREXONE HYDROCHLORIDE TABLET, FILM COATED [BRYANT RANCH PREPACK]1001
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTTRIAMTERENE HYDROCHLOROTHIAZIDE (TRIAMTERENE AND HYDROCHLOROTHIAZIDE) TABLET [BRYANT RANCH PREPACK]1001
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTLEVOFLOXACIN TABLET, FILM COATED [BRYANT RANCH PREPACK]1000
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTPANTOPRAZOLE SODIUM TABLET, DELAYED RELEASE [BRYANT RANCH PREPACK]1000
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTREQUIP (ROPINIROLE) TABLET, FILM COATED [BRYANT RANCH PREPACK]1000
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTPROTONIX DELAYED-RELEASE (PANTOPRAZOLE SODIUM) TABLET, DELAYED RELEASE PROTONIX DELAYED-RELEASE (PANTOPRAZOLE SODIUM) GRANULE, DELAYED RELEASE [WYETH PHARMACEUTICALS INC., A SUBSIDIARY OF PFIZER INC.]26
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTGLYBURIDE AND METFORMIN HYDROCHLORIDE TABLET, FILM COATED [TEVA PHARMACEUTICALS USA INC]19
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTDESIPRAMINE HYDROCHLORIDE TABLET, FILM COATED [SANDOZ INC]18
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTMIRTAZAPINE TABLET, FILM COATED [ACTAVIS PHARMA, INC.]18
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTRANITIDINE HYDROCHLORIDE CAPSULE RANITIDINE HYDROCHLORIDE TABLET, FILM COATED [SANDOZ INC]18
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTAMOXICILLIN AND CLAVULANATE POTASSIUM TABLET, FILM COATED AMOXICILLIN AND CLAVULANATE POTASSIUM POWDER, FOR SUSPENSION AMOXICILLIN AND CLAVULANATE POTASSIUM TABLET, CHEWABLE [TEVA PHARMACEUTICALS USA INC]16
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTARICEPT (DONEPEZIL HYDROCHLORIDE) TABLET, FILM COATED ARICEPT ODT (DONEPEZIL HYDROCHLORIDE) TABLET, ORALLY DISINTEGRATING [EISAI INC.]16
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTTROSPIUM CHLORIDE CAPSULE, EXTENDED RELEASE [ACTAVIS PHARMA, INC.]16
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTBENAZEPRIL HYDROCHLORIDE TABLET, FILM COATED [AUROBINDO PHARMA LIMITED]15
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTCLARITHROMYCIN TABLET [PD-RX PHARMACEUTICALS, INC.]15
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTCLARITHROMYCIN TABLET [SANDOZ INC]15
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTLANSOPRAZOLE, AMOXICILLIN AND CLARITHROMYCIN KIT [SANDOZ INC]15
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTLEVETIRACETAM TABLET, FILM COATED [AUROBINDO PHARMA LIMITED]15
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTTOPIRAMATE TABLET, FILM COATED TOPIRAMATE (TOPIRAMATE ) TABLET, FILM COATED [AUROBINDO PHARMA LIMITED]15
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTTRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN TABLET, FILM COATED [MICRO LABS LIMITED]15
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTCIPROFLOXACIN TABLET, FILM COATED [IVAX PHARMACEUTICALS, INC.]14
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTPAROXETINE (PAROXETINE HYDROCHLORIDE) TABLET, FILM COATED [AUROBINDO PHARMA LIMITED]14
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTCEPHALEXIN CAPSULE CEPHALEXIN POWDER, FOR SUSPENSION CEPHALEXIN TABLET [TEVA PHARMACEUTICALS USA INC]13
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTCIPROFLOXACIN TABLET, FILM COATED, EXTENDED RELEASE [WATSON PHARMA, INC.]13
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTQUINAPRIL HYDROCHLORIDE/HYDROCHLOROTHIAZIDE TABLET, FILM COATED [AUROBINDO PHARMA LIMITED]13
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTMONTELUKAST SODIUM GRANULE [DR.REDDY'S LABORATORIES LIMITED]12
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENTPERPHENAZINE TABLET, FILM COATED [SANDOZ INC]12

Inactive Ingredient Database#

Browse recovered IID releases and source provenance.

Current IID rows for UNII 0VUT3PMY82 page 1 of 1 ยท 15 matching rows.

Ingredient, UNII, CAS table
IngredientUNIICASDosage formRoutePotencyMaximum daily exposure
HYPROMELLOSE 2910 (3 MPA.S)0VUT3PMY829004653SOLUTION/ DROPSOPHTHALMIC0.5 %w/v
HYPROMELLOSE 2910 (3 MPA.S)0VUT3PMY829004653CAPSULEORAL400 mg
HYPROMELLOSE 2910 (3 MPA.S)0VUT3PMY829004653CAPSULE, DELAYED RELEASEORAL721 mg
HYPROMELLOSE 2910 (3 MPA.S)0VUT3PMY829004653CAPSULE, EXTENDED RELEASEORAL105 mg
HYPROMELLOSE 2910 (3 MPA.S)0VUT3PMY829004653GRANULEORAL295 mg
HYPROMELLOSE 2910 (3 MPA.S)0VUT3PMY829004653GRANULE, FOR SUSPENSIONORAL1 mg
HYPROMELLOSE 2910 (3 MPA.S)0VUT3PMY829004653SUSPENSIONORAL156 mg
HYPROMELLOSE 2910 (3 MPA.S)0VUT3PMY829004653TABLETORAL570 mg
HYPROMELLOSE 2910 (3 MPA.S)0VUT3PMY829004653TABLET, DELAYED RELEASEORAL140 mg
HYPROMELLOSE 2910 (3 MPA.S)0VUT3PMY829004653TABLET, EXTENDED RELEASEORAL231 mg
HYPROMELLOSE 2910 (3 MPA.S)0VUT3PMY829004653TABLET, FILM COATEDORAL78 mg
HYPROMELLOSE 2910 (3 MPA.S)0VUT3PMY829004653TABLET, FILM COATED, EXTENDED RELEASEORAL8 mg
HYPROMELLOSE 2910 (3 MPA.S)0VUT3PMY829004653TABLET, FOR SUSPENSIONORAL250 mg
HYPROMELLOSE 2910 (3 MPA.S)0VUT3PMY829004653TABLET, ORALLY DISINTEGRATINGORAL52 mg
HYPROMELLOSE 2910 (3 MPA.S)0VUT3PMY829004653TABLET, ORALLY DISINTEGRATING, DELAYED RELEASEORAL36 mg