CYCLOBENZAPRINE HYDROCHLORIDE

Product NDC
70518-2788
11-digit product format
705182788
Labeler code
70518
Product ID
70518-2788_d4fffb51-6fd8-bdc9-e053-2995a90a7268
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
cyclobenzaprine hydrochloride
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
REMEDYREPACK INC.
Application
ANDA208170
Marketing category
ANDA
Marketing start
2020-06-16
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
70518-2788-07051827880030 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2788-0) 2020-06-160000-00-00NoNoCurrent
70518-2788-17051827880130 TABLET, FILM COATED in 1 BLISTER PACK (70518-2788-1) 2020-07-130000-00-00NoNoCurrent
70518-2788-27051827880290 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2788-2) 2020-07-280000-00-00NoNoCurrent
70518-2788-37051827880360 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2788-3) 2020-07-280000-00-00NoNoCurrent
70518-2788-4705182788046 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2788-4) 2021-09-100000-00-00NoNoCurrent
70518-2788-57051827880590 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2788-5) 2021-10-130000-00-00NoNoCurrent
70518-2788-67051827880630 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2788-6) 2021-11-150000-00-00NoNoCurrent
70518-2788-77051827880710 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2788-7) 2021-12-060000-00-00NoNoCurrent
70518-2788-87051827880815 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2788-8) 2022-01-060000-00-00NoNoCurrent