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HYPROMELLOSE 2910 (10000 MPA.S)

Substance profile for UNII 0HO1H52958, enriched with FDA NDC listings, DailyMed labels, legacy aliases, and open chemistry identifiers.

Substance Identity#

UNII
0HO1H52958
Preferred term
HYPROMELLOSE 2910 (10000 MPA.S)
Registry number
9004-65-3
Ingredient type
INGREDIENT SUBSTANCE
Molecular formula
Polymer substance not supported

Chemical And Database Identifiers#

RxCUI
1437983
PubChem
0
INN ID
0

Open Chemistry Sources#

Source, Identifier, Link table
SourceIdentifierLink
RxNorm1437983mor.nlm.nih.gov/RxNav/search?searchBy=RXCUI&searchTerm=1437983
FDA Substance Registration System0HO1H52958precision.fda.gov/uniisearch/srs/unii/0HO1H52958

DailyMed Socrata Ingredients#

DailyMed label, SPL version table
DailyMed labelSPL version
These highlights do not include all the information needed to use zolmitriptan tablets safely and effectively. See full prescribing information for zolmitriptan tablets. ZOLMITRIPTAN Tablets, for Oral Use Initial U.S. Approval: 19972
2a7af445-83f2-4da3-8df0-51bd808f86121
DEMECLOCYCLINE HYDROCHLORIDE TABLET, FILM COATED [EPIC PHARMA, LLC]3
NIACIN TABLET, EXTENDED RELEASE [TEVA PHARMACEUTICALS USA INC]3

Inactive Ingredient Database#

Browse recovered IID releases and source provenance.

Current IID rows for UNII 0HO1H52958 page 1 of 1 ยท 4 matching rows.

Ingredient, UNII, CAS table
IngredientUNIICASDosage formRoutePotencyMaximum daily exposure
HYPROMELLOSE 2910 (10000 MPA.S)0HO1H529589004653SOLUTIONORAL74 mg
HYPROMELLOSE 2910 (10000 MPA.S)0HO1H529589004653TABLETORAL188 mg
HYPROMELLOSE 2910 (10000 MPA.S)0HO1H529589004653TABLET, EXTENDED RELEASEORAL524 mg
HYPROMELLOSE 2910 (10000 MPA.S)0HO1H529589004653GELVAGINAL175 mg