Precose

Product NDC
50419-861
11-digit product format
504190861
Labeler code
50419
Product ID
50419-861_61dbcee7-11a4-4d8c-8e2c-7cbab79b2871
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Acarbose
Dosage form
TABLET
Route
ORAL
Labeler
Bayer HealthCare Pharmaceuticals Inc.
Application
NDA020482
Marketing category
NDA
Marketing start
2008-01-30
Marketing end
0000-00-00
Substance
ACARBOSE
Active strength
50 mg/1
Pharmacologic classes
alpha Glucosidase Inhibitors [MoA],alpha-Glucosidase Inhibitor [EPC]
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
2712f130-8721-1a9d-6846-53893b13fb67Product name220210312

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
50419-861-512022-10-11C16284748780-1ba0f9c33-3144-a910-e053-dadaa90a0b8529a6f213-bc93-4dbd-bab0-744722b6f0b8
50419-861-512021-01-29C16284748780-1ba0f9c33-3144-a910-e053-dadaa90a0b8529a6f213-bc93-4dbd-bab0-744722b6f0b8

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
50419-861-48EA - Each50419-8615104fb30-536f-4504-9f61-576e2dc8a49e12012-07-24
50419-861-51EA - Each50419-861cbfa17c5-66cb-4fe2-8469-48d7d96c804412012-07-24

DailyMed Socrata Ingredients#

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
199149acarbose 50 MG Oral TabletPSNc85bc02a-bf18-4690-84b8-2c256bce5f9f1
209247PRECOSE 50 MG Oral TabletPSNc85bc02a-bf18-4690-84b8-2c256bce5f9f1
209247acarbose 50 MG Oral Tablet [Precose]SBDc85bc02a-bf18-4690-84b8-2c256bce5f9f1
199149acarbose 50 MG Oral TabletSCDc85bc02a-bf18-4690-84b8-2c256bce5f9f1
209247Precose 50 MG Oral TabletSYc85bc02a-bf18-4690-84b8-2c256bce5f9f1