Propranolol Hydrochloride

Product NDC
0615-7761
11-digit product format
006157761
Labeler code
0615
Product ID
0615-7761_767c21f7-8cfc-42fa-8426-8baa18752ab1
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Propranolol Hydrochloride
Dosage form
TABLET
Route
ORAL
Labeler
NCS HealthCare of KY, Inc dba Vangard Labs
Application
ANDA071972
Marketing category
ANDA
Marketing start
1990-09-30
Marketing end
0000-00-00
Substance
PROPRANOLOL HYDROCHLORIDE
Active strength
10 mg/1
Pharmacologic classes
Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0615-7761-392021-08-11C16284748780-19d75b9d0-1042-f424-e053-dadaa90a57ce7f56b4fd-8200-4546-977d-6d0960aaa766
0615-7761-392020-01-31C16284748780-19d75b9d0-1042-f424-e053-dadaa90a57ce7f56b4fd-8200-4546-977d-6d0960aaa766