Fluticasone Propionate

Product NDC: 69306-016
11-digit product format: 693060016
Labeler code: 69306
Product ID: 69306-016_eb848fb7-9c35-ea59-e053-2a95a90ac3ce
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Fluticasone Propionate
Dosage form: SPRAY, METERED
Route: NASAL
Labeler: Doc Rx
Application: ANDA077570
Marketing category: ANDA
Marketing start: 2008-01-16
Marketing end: 0000-00-00
Substance: FLUTICASONE PROPIONATE
Active strength: 50 ug/.1g
Pharmacologic classes: Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
NDC exclude flag: No
Listing certified through: 2023-12-31
Current FDA listing: Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
69306-016-01	2024-12-06	C162847	48780-1	1030e364-ff30-111a-e063-dadaa90a10e2	9a922971-50e7-4e76-81c0-e430e4342bcb
69306-016-01	2024-07-30	C162847	48780-1	1030e364-ff30-111a-e063-dadaa90a10e2	9a922971-50e7-4e76-81c0-e430e4342bcb
69306-016-01	2024-01-30	C162847	48780-1	1030e364-ff30-111a-e063-dadaa90a10e2	9a922971-50e7-4e76-81c0-e430e4342bcb

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
69306-016-01	GM - Gram	69306-016	a73b6814-f6d0-4659-bbc8-607ba1c286a8	1	2021-10-08

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
O2GMZ0LF5W	FLUTICASONE PROPIONATE	80474-14-2	FLUTICASONE PROPIONATE

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
69306-016-01	69306001601	16 g in 1 BOTTLE, PUMP (69306-016-01)	16 g	2020-02-18	0000-00-00	No	No	Current