Doxycycline

Product NDC: 49884-726
11-digit product format: 498840726
Labeler code: 49884
Product ID: 49884-726_da765403-ebf9-4189-894d-61678ab69965
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: doxycycline
Dosage form: CAPSULE
Route: ORAL
Labeler: Par Pharmaceutical, Inc.
Application: ANDA065055
Marketing category: ANDA
Marketing start: 2000-12-01
Marketing end: 2024-11-30
Substance: DOXYCYCLINE
Active strength: 50 mg/1
Pharmacologic classes: Tetracycline-class Drug [EPC], Tetracyclines [CS]
NDC exclude flag: No
Listing certified through: 0000-00-00
Current FDA listing: Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
49884-726-01	2022-08-25	C162847	48780-1	e4f33bdf-a902-d8a0-e053-dadaa90a6e4e	4ae0ff63-c577-478e-9fa0-b7c22a8e7de4
49884-726-01	2022-07-29	C162847	48780-1	e4f33bdf-a902-d8a0-e053-dadaa90a6e4e	4ae0ff63-c577-478e-9fa0-b7c22a8e7de4

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
49884-726-01	EA - Each	49884-726	83866ddd-2ce7-4c11-958a-cd56d01f8314	1	2012-07-24

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
49884-726-01	49884072601	100 CAPSULE in 1 BOTTLE (49884-726-01)	100 capsule	2000-12-01	0000-00-00	No	No	Current