CYCLOBENZAPRINE HYDROCHLORIDE

Product NDC
71335-1089
11-digit product format
713351089
Labeler code
71335
Product ID
71335-1089_fb51afd9-e542-4a23-9f67-f8a0e417a986
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
CYCLOBENZAPRINE HYDROCHLORIDE
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA078218
Marketing category
ANDA
Marketing start
2010-02-18
Marketing end
0000-00-00
Substance
CYCLOBENZAPRINE HYDROCHLORIDE
Active strength
10 mg/1
Pharmacologic classes
Centrally-mediated Muscle Relaxation [PE], Muscle Relaxant [EPC]
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
71335-1089-07133510890040 TABLET, FILM COATED in 1 BOTTLE (71335-1089-0) 2019-02-080000-00-00NoNoCurrent
71335-1089-17133510890114 TABLET, FILM COATED in 1 BOTTLE (71335-1089-1) 2019-02-080000-00-00NoNoCurrent
71335-1089-27133510890284 TABLET, FILM COATED in 1 BOTTLE (71335-1089-2) 2019-02-080000-00-00NoNoCurrent
71335-1089-37133510890330 TABLET, FILM COATED in 1 BOTTLE (71335-1089-3) 2019-02-080000-00-00NoNoCurrent
71335-1089-47133510890420 TABLET, FILM COATED in 1 BOTTLE (71335-1089-4) 2019-02-080000-00-00NoNoCurrent
71335-1089-57133510890515 TABLET, FILM COATED in 1 BOTTLE (71335-1089-5) 2019-02-080000-00-00NoNoCurrent
71335-1089-67133510890660 TABLET, FILM COATED in 1 BOTTLE (71335-1089-6) 2019-02-080000-00-00NoNoCurrent
71335-1089-77133510890790 TABLET, FILM COATED in 1 BOTTLE (71335-1089-7) 2019-02-080000-00-00NoNoCurrent
71335-1089-87133510890856 TABLET, FILM COATED in 1 BOTTLE (71335-1089-8) 2019-02-080000-00-00NoNoCurrent
71335-1089-971335108909120 TABLET, FILM COATED in 1 BOTTLE (71335-1089-9) 2019-02-080000-00-00NoNoCurrent