NDC 16714-977-01 - propofol

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC: 16714-977
Requested NDC: 16714-977-01
Package NDCs from labels: 16714-977-01, 16714-977-20
Manufacturer: NorthStar Rx LLC
Effective date: 2026-09-22
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
propofol - NorthStar Rx LLC	NorthStar Rx LLC	2026-09-22	HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
16714-977-01	propofol	50 mL in 1 VIAL	INJECTION, EMULSION	50		5
16714-977-20	propofol	20 in 1 CARTON	INJECTION, EMULSION	20		5

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
16714-977	PROPOFOL INJECTION, EMULSION [NORTHSTAR RX LLC]	4	Current NDC, Legacy NDC, 2 package rows	20241207_5ec25932-6c21-4cd5-8f60-80761f2e20a6.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
16714-977-01	ML - Milliliter	16714-977	96a9fdf0-9e3e-423e-9869-e4a21ead5918	1	2022-09-12
16714-977-20	ML - Milliliter	16714-977	1cf70723-d83c-4b2c-bc7b-9c767e776127	1	2022-09-12

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 26 of 26 · 502 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Eye Wash	WATER	CVS Pharmacy	049cee29-7ec2-4d5b-8308-f522acde43a7	2017-03-29	Warnings	Exact identifier unii: 059QF0KO0R
Sterile Water	WATER	Baxter Healthcare Company	210dc9ab-d6ca-4552-ac19-1be17792d290	2016-05-31	Warnings, Adverse reactions	Exact identifier unii: 059QF0KO0R

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.