NDC 55529-021 - Norocillin

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: 55529-021
Package NDCs from labels: 55529-021-02, 55529-021-04, 55529-021-05
Manufacturer: Norbrook Laboratories Limited
Effective date: 2025-01-27
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Norocillin - Norbrook Laboratories Limited	Norbrook Laboratories Limited	2025-01-27	PRESCRIPTION ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
55529-021-02	Norocillin	100 mL in 1 VIAL, GLASS	INJECTION, SUSPENSION	100	6
55529-021-04	Norocillin	250 mL in 1 VIAL, GLASS	INJECTION, SUSPENSION	250	6
55529-021-05	Norocillin	500 mL in 1 VIAL, GLASS	INJECTION, SUSPENSION	500	6

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
55529-021	NOROCILLIN (PENICILLIN G PROCAINE) INJECTION, SUSPENSION [NORBROOK LABORATORIES LIMITED]	6	3 package rows	20250129_0116d56d-53f8-429e-b0fc-5319af7fe903.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
penicillin G procaine	ACTIVE INGREDIENT	17R794ESYN	NOROCILLIN (PENICILLIN G PROCAINE) INJECTION, SUSPENSION [NORBROOK LABORATORIES LIMITED]	2
penicillin G procaine	ACTIVE MOIETY	17R794ESYN	NOROCILLIN (PENICILLIN G PROCAINE) INJECTION, SUSPENSION [NORBROOK LABORATORIES LIMITED]	2
carboxymethylcellulose sodium	INACTIVE INGREDIENT	K679OBS311	NOROCILLIN (PENICILLIN G PROCAINE) INJECTION, SUSPENSION [NORBROOK LABORATORIES LIMITED]	2
lecithin, soybean	INACTIVE INGREDIENT	1DI56QDM62	NOROCILLIN (PENICILLIN G PROCAINE) INJECTION, SUSPENSION [NORBROOK LABORATORIES LIMITED]	2
methylparaben	INACTIVE INGREDIENT	A2I8C7HI9T	NOROCILLIN (PENICILLIN G PROCAINE) INJECTION, SUSPENSION [NORBROOK LABORATORIES LIMITED]	2
penicillin G potassium	INACTIVE INGREDIENT	VL775ZTH4C	NOROCILLIN (PENICILLIN G PROCAINE) INJECTION, SUSPENSION [NORBROOK LABORATORIES LIMITED]	2
polysorbate 80	INACTIVE INGREDIENT	6OZP39ZG8H	NOROCILLIN (PENICILLIN G PROCAINE) INJECTION, SUSPENSION [NORBROOK LABORATORIES LIMITED]	2
potassium phosphate, dibasic	INACTIVE INGREDIENT	CI71S98N1Z	NOROCILLIN (PENICILLIN G PROCAINE) INJECTION, SUSPENSION [NORBROOK LABORATORIES LIMITED]	2
potassium phosphate, monobasic	INACTIVE INGREDIENT	4J9FJ0HL51	NOROCILLIN (PENICILLIN G PROCAINE) INJECTION, SUSPENSION [NORBROOK LABORATORIES LIMITED]	2
procaine hydrochloride	INACTIVE INGREDIENT	95URV01IDQ	NOROCILLIN (PENICILLIN G PROCAINE) INJECTION, SUSPENSION [NORBROOK LABORATORIES LIMITED]	2
sodium formaldehyde sulfoxylate	INACTIVE INGREDIENT	X4ZGP7K714	NOROCILLIN (PENICILLIN G PROCAINE) INJECTION, SUSPENSION [NORBROOK LABORATORIES LIMITED]	2
water	INACTIVE INGREDIENT	059QF0KO0R	NOROCILLIN (PENICILLIN G PROCAINE) INJECTION, SUSPENSION [NORBROOK LABORATORIES LIMITED]	2

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 25 of 28 · 541 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Kali phosphoricum	DIBASIC POTASSIUM PHOSPHATE	Boiron	860a5c8e-6d7b-e64d-e053-2991aa0af802	2023-01-23		Exact identifier unii: CI71S98N1Z
Rehydrate	AVENA SATIVA, EQUISETUM HYEMALE, HYPERICUM PERFORATUM, ULMUS FULVA, GLYCYRRHIZA GLABRA, SILICEA, PUERARIA LOBATA, CARLSBAD AQUA, ADENOSINUM TRIPHOSPHORICUM DINATRUM, GERMANIUM SESQUIOXIDE, HYDROGEN, OXYGEN, WIESBADEN	ParaDocs All Natural, Inc.	648fab10-c46b-420f-a42c-6642009d83fb	2023-01-10	Warnings	Exact identifier unii: 059QF0KO0R
Kali phosphoricum	DIBASIC POTASSIUM PHOSPHATE	Boiron	860aa384-8552-7a57-e053-2991aa0a43aa	2023-01-06		Exact identifier unii: CI71S98N1Z
Sleep	HYOSCYAMUS NIGER, STRYCHNOS IGNATII SEED, AND POTASSIUM PHOSPHATE, DIBASIC	Hyland's Inc.	8ad9775f-367c-45c9-890d-69a3734965f1	2022-12-14	Warnings	Exact identifier unii: CI71S98N1Z
Kali Phos	DIBASIC POTASSIUM PHOSPHATE	Hylands Inc.	d398ba78-c986-9f9a-e053-2995a90ace53	2022-12-12	Warnings	Exact identifier unii: CI71S98N1Z
CALMS FORTE	AVENA SATIVA FLOWERING TOP, TRIBASIC CALCIUM PHOSPHATE, MATRICARIA RECUTITA, FERROSOFERRIC PHOSPHATE, HOPS, POTASSIUM PHOSPHATE, DIBASIC, MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE, SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE, AND PASSIFLORA INCARNATA FLOWER	Hyland's Inc.	f48a35d4-aa0c-48b1-a2ad-a614ea2894e8	2022-12-07	Warnings	Exact identifier unii: CI71S98N1Z
Refresh Digital PF	CARBOXYMETHYLCELLULOSE SODIUM, GLYCERIN AND POLYSORBATE 80	Allergan, Inc.	97e83e68-6374-4df4-93f6-d707fc32748d	2022-11-28	Warnings	Exact identifier unii: 6OZP39ZG8H unii: K679OBS311
Refresh Digital	CARBOXYMETHYLCELLULOSE SODIUM, GLYCERIN, POLYSORBATE 80	Allergan, Inc.	b2bd34d4-fab9-4f4b-9be2-5d30b55f5b81	2022-11-28	Warnings	Exact identifier unii: 6OZP39ZG8H unii: K679OBS311
Sterile Water	WATER	Fresenius Kabi USA, LLC	b45e9f1d-9c48-4b46-8541-d846b89540df	2022-10-26	Warnings, Adverse reactions	Exact identifier unii: 059QF0KO0R
Kali Phosphoricum	KALI PHOSPHORICUM	Hahnemann Laboratories, INC.	eb6ac6ad-4677-1072-e053-2995a90a02e9	2022-10-19		Exact identifier unii: CI71S98N1Z
Eye wash	PURIFIED WATER	McKesson	bd089fde-24ba-4de5-e053-2995a90a39bb	2022-10-18	Warnings	Exact identifier unii: 059QF0KO0R
Bach Original Flower Remedies Rock Water	WATER	Nelson Bach USA Limited	ea242559-1618-3354-e053-2a95a90a1a95	2022-10-03	Warnings	Exact identifier unii: 059QF0KO0R
REFRESH OPTIVE	CARBOXYMETHYLCELLULOSE SODIUM AND GLYCERIN	Allergan, Inc.	7f8d88af-fd3b-4138-af61-f24c59ccebd7	2022-09-23	Warnings	Exact identifier unii: K679OBS311
Sterile Water	WATER	Medical Purchasing Solutions, LLC	e90b47e3-9636-b9ee-e053-2a95a90ad48c	2022-09-19	Warnings, Adverse reactions	Exact identifier unii: 059QF0KO0R
REFRESH OPTIVE Advanced	CARBOXYMETHYLCELLULOSE SODIUM, GLYCERIN, POLYSORBATE 80	Allergan, Inc.	ebd0839e-2e1d-4e0e-986c-19f1f5c76358	2022-09-15	Warnings	Exact identifier unii: 6OZP39ZG8H unii: K679OBS311
REFRESH OPTIVE Advanced	CARBOXYMETHYLCELLULOSE SODIUM, GLYCERIN, AND POLYSORBATE 80	Allergan, Inc.	aaa943e4-7c38-4c5a-b7c0-5a656d8cafc0	2022-09-01	Warnings	Exact identifier unii: 6OZP39ZG8H unii: K679OBS311
REFRESH TEARS	CARBOXYMETHYLCELLULOSE SODIUM	Allergan, Inc.	329d1fe0-4432-4565-b7b1-65666bd86526	2022-06-30	Warnings	Exact identifier unii: K679OBS311
REFRESH Optive Mega-3	CARBOXYMETHYLCELLULOSE SODIUM, GLYCERIN AND POLYSORBATE 80	Allergan, Inc.	c5f2b3f2-2071-45bd-a010-67f848bc0233	2022-06-30	Warnings	Exact identifier unii: 6OZP39ZG8H unii: K679OBS311
REFRESH PLUS	CARBOXYMETHYLCELLULOSE SODIUM	Allergan, Inc.	0f6a4b4b-cde6-4518-84b5-ce997f1154a7	2022-06-28	Warnings	Exact identifier unii: K679OBS311
Sterile Water	WATER	Fresenius Kabi USA, LLC	f42ac50f-0ec5-4713-a4c8-99d972d90bed	2022-06-22	Warnings, Adverse reactions	Exact identifier unii: 059QF0KO0R

Reported adverse events (FAERS/openFDA)#

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