Propranolol Hydrochloride

Product NDC
63629-6310
11-digit product format
636296310
Labeler code
63629
Product ID
63629-6310_3c133f96-d4ef-4ee8-8707-2ad3114f29e8
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Propranolol Hydrochloride
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA071972
Marketing category
ANDA
Marketing start
1990-09-30
Marketing end
0000-00-00
Substance
PROPRANOLOL HYDROCHLORIDE
Active strength
40 mg/1
Pharmacologic classes
Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
63629-6310-12021-04-23C16284748780-19d75b9d0-ba2e-f424-e053-dadaa90a57cedac7912c-159e-40f4-8849-4d4a55c96efb
63629-6310-12020-01-31C16284748780-19d75b9d0-ba2e-f424-e053-dadaa90a57cedac7912c-159e-40f4-8849-4d4a55c96efb