Morphine Sulfate

Product NDC
55700-552
11-digit product format
557000552
Labeler code
55700
Product ID
55700-552_640b8ee2-a3aa-4b05-a863-01fb09c4c29e
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Morphine Sulfate
Dosage form
CAPSULE, EXTENDED RELEASE
Route
ORAL
Labeler
Lake Erie Medical DBA Quality Care Products LLC
Application
ANDA202104
Marketing category
ANDA
Marketing start
2017-08-18
Marketing end
0000-00-00
Substance
MORPHINE SULFATE
Active strength
50 mg/1
Pharmacologic classes
Full Opioid Agonists [MoA],Opioid Agonist [EPC]
DEA schedule
CII
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
55700-552-602021-04-15C16284748780-1ba0f9c33-4fa6-a910-e053-dadaa90a0b85f1845c76-8c8c-40a1-a145-78338649925e
55700-552-602021-01-29C16284748780-1ba0f9c33-4fa6-a910-e053-dadaa90a0b85f1845c76-8c8c-40a1-a145-78338649925e

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
55700-552-60EA - Each55700-552fe1e9c9d-8cf8-46ed-8139-7b0e6c919a2d12017-10-13