Doxycycline Hyclate

Product NDC: 63739-168
11-digit product format: 637390168
Labeler code: 63739
Product ID: 63739-168_b8cccdd0-3949-176a-e053-2a95a90ae65f
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Doxycycline Hyclate
Dosage form: TABLET
Route: ORAL
Labeler: McKesson Corporation dba SKY Packaging
Application: ANDA062421
Marketing category: ANDA
Marketing start: 1990-01-01
Marketing end: 0000-00-00
Substance: DOXYCYCLINE HYCLATE
Active strength: 100 mg/1
Pharmacologic classes: Tetracycline-class Drug [EPC],Tetracyclines [CS]
NDC exclude flag: No
Listing certified through: 2022-12-31
Current FDA listing: Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
63739-168-33	2020-07-22	C162847	48780-1	ab0e2407-2750-f274-e053-dbdaa90a6471	3a70a0da-181f-48d3-96e4-747d56251fc2

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
63739-168-33	EA - Each	63739-168	efdf9314-2534-450e-8b78-ccb7cc8cdc4a	1	2016-04-04

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
63739-168-33	63739016833	3 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-168-33) > 10 TABLET in 1 BLISTER PACK	3 blister pack	2016-03-29	0000-00-00	No	No	Current