Metoclopramide Hydrochloride

Product NDC
63739-293
11-digit product format
637390293
Labeler code
63739
Product ID
63739-293_9dfd93a6-24d8-490a-9388-db3c3d736adb
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Metoclopramide Hydrochloride
Dosage form
TABLET
Route
ORAL
Labeler
McKesson Corporation dba SKY Packaging
Application
ANDA071250
Marketing category
ANDA
Marketing start
2011-08-22
Marketing end
0000-00-00
Substance
METOCLOPRAMIDE HYDROCHLORIDE
Active strength
10 mg/1
Pharmacologic classes
Dopamine D2 Antagonists [MoA],Dopamine-2 Receptor Antagonist [EPC]
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
63739-293-102020-07-22C16284748780-1ab0e2407-2708-f274-e053-dbdaa90a647103f383e4-352b-46b3-af63-644e63702b68

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
63739-293-10EA - Each63739-2930782d774-672c-44c2-9628-3651a1dae33012015-12-02