NDC 0703-3301-01 - Octreotide Acetate

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: 0703-3301
Requested NDC: 0703-3301-01
Package NDCs from labels: 0703-3301-01, 0703-3301-04
Manufacturer: Teva Parenteral Medicines, Inc.
Effective date: 2023-02-28
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Octreotide Acetate Injection Rx only	Teva Parenteral Medicines, Inc.	2023-02-28	HUMAN PRESCRIPTION DRUG LABEL

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
0703-3301-04	ML - Milliliter	0703-3301	61e88fad-a44a-45a5-8776-3f6b3fa80c48	1	2012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
OCTREOTIDE ACETATE	ACTIVE INGREDIENT	75R0U2568I	OCTREOTIDE ACETATE INJECTION, SOLUTION [TEVA PARENTERAL MEDICINES, INC.]	3
OCTREOTIDE	ACTIVE MOIETY	RWM8CCW8GP	OCTREOTIDE ACETATE INJECTION, SOLUTION [TEVA PARENTERAL MEDICINES, INC.]	3
ACETIC ACID	INACTIVE INGREDIENT	Q40Q9N063P	OCTREOTIDE ACETATE INJECTION, SOLUTION [TEVA PARENTERAL MEDICINES, INC.]	3
MANNITOL	INACTIVE INGREDIENT	3OWL53L36A	OCTREOTIDE ACETATE INJECTION, SOLUTION [TEVA PARENTERAL MEDICINES, INC.]	3
PHENOL	INACTIVE INGREDIENT	339NCG44TV	OCTREOTIDE ACETATE INJECTION, SOLUTION [TEVA PARENTERAL MEDICINES, INC.]	3
SODIUM ACETATE	INACTIVE INGREDIENT	4550K0SC9B	OCTREOTIDE ACETATE INJECTION, SOLUTION [TEVA PARENTERAL MEDICINES, INC.]	3
WATER	INACTIVE INGREDIENT	059QF0KO0R	OCTREOTIDE ACETATE INJECTION, SOLUTION [TEVA PARENTERAL MEDICINES, INC.]	3

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 20 of 20 · 382 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.