Doxycycline

Product NDC
71335-2109
11-digit product format
713352109
Labeler code
71335
Product ID
71335-2109_f1057e47-64bd-440e-a2db-59d161081534
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Doxycycline
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA065285
Marketing category
ANDA
Marketing start
2005-12-08
Marketing end
0000-00-00
Substance
DOXYCYCLINE
Active strength
100 mg/1
Pharmacologic classes
Tetracycline-class Drug [EPC], Tetracyclines [CS]
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
71335-2109-0713352109002 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2109-0) 2022-06-060000-00-00NoNoCurrent
71335-2109-17133521090130 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2109-1) 2022-06-060000-00-00NoNoCurrent
71335-2109-27133521090214 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2109-2) 2022-06-060000-00-00NoNoCurrent
71335-2109-37133521090320 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2109-3) 2022-06-060000-00-00NoNoCurrent
71335-2109-47133521090412 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2109-4) 2022-06-060000-00-00NoNoCurrent
71335-2109-57133521090540 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2109-5) 2022-06-060000-00-00NoNoCurrent
71335-2109-67133521090610 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2109-6) 2022-06-060000-00-00NoNoCurrent
71335-2109-77133521090750 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2109-7) 2022-06-060000-00-00NoNoCurrent
71335-2109-87133521090821 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2109-8) 2022-06-060000-00-00NoNoCurrent
71335-2109-97133521090960 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2109-9) 2022-06-060000-00-00NoNoCurrent