Propranolol Hyrochloride

Product NDC: 51655-318
11-digit product format: 516550318
Labeler code: 51655
Product ID: 51655-318_43f30617-de6a-47e3-a715-e41f45b20d14
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Propranolol Hydrochloride
Dosage form: TABLET
Route: ORAL
Labeler: Northwind Pharmaceuticals
Application: ANDA070213
Marketing category: ANDA
Marketing start: 2014-05-15
Marketing end: 0000-00-00
Substance: PROPRANOLOL HYDROCHLORIDE
Active strength: 10 mg/301
Pharmacologic classes: Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]
NDC exclude flag: E
Listing certified through: 2018-12-31
Current FDA listing: Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
51655-318-52	2026-01-06	C162847	48780-1	9d75b9cf-f7d0-f424-e053-dadaa90a57ce	024003d4-eb1f-4537-92f8-555cf1f354dc
51655-318-52	2020-01-31	C162847	48780-1	9d75b9cf-f7d0-f424-e053-dadaa90a57ce	024003d4-eb1f-4537-92f8-555cf1f354dc

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version	Uploaded
PROPRANOLOL HYDROCHLORIDE	ACTIVE INGREDIENT	F8A3652H1V	PROPRANOLOL HYROCHLORIDE (PROPRANOLOL HYDROCHLORIDE) TABLET [NORTHWIND PHARMACEUTICALS]	1
PROPRANOLOL	ACTIVE MOIETY	9Y8NXQ24VQ	PROPRANOLOL HYROCHLORIDE (PROPRANOLOL HYDROCHLORIDE) TABLET [NORTHWIND PHARMACEUTICALS]	1

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
51655-318	PROPRANOLOL HYROCHLORIDE (PROPRANOLOL HYDROCHLORIDE) TABLET [NORTHWIND PHARMACEUTICALS]	1	Legacy NDC	20140516_024003d4-eb1f-4537-92f8-555cf1f354dc.zip