FDA.reportPublic FDA data

Fexmid

Product NDC
55700-726
11-digit product format
557000726
Labeler code
55700
Product ID
55700-726_98213ac9-6309-4027-95ca-149fb0770e27
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Cyclobenzaprine Hydrochloride
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Quality Care Products, LLC
Application
ANDA071611
Marketing category
ANDA
Marketing start
2019-02-15
Marketing end
0000-00-00
Substance
CYCLOBENZAPRINE HYDROCHLORIDE
Active strength
8 mg/1
Pharmacologic classes
Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC]
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
55700-726-302025-01-10C16284748780-1ba0f9c33-2eb9-a910-e053-dadaa90a0b85e7649bf8-266d-4ef2-aaea-ae12a1f6bcd6
55700-726-602025-01-10C16284748780-1ba0f9c33-2eb9-a910-e053-dadaa90a0b85e7649bf8-266d-4ef2-aaea-ae12a1f6bcd6
55700-726-902025-01-10C16284748780-1ba0f9c33-2eb9-a910-e053-dadaa90a0b85e7649bf8-266d-4ef2-aaea-ae12a1f6bcd6
55700-726-302021-01-29C16284748780-1ba0f9c33-2eb9-a910-e053-dadaa90a0b85e7649bf8-266d-4ef2-aaea-ae12a1f6bcd6
55700-726-602021-01-29C16284748780-1ba0f9c33-2eb9-a910-e053-dadaa90a0b85e7649bf8-266d-4ef2-aaea-ae12a1f6bcd6
55700-726-902021-01-29C16284748780-1ba0f9c33-2eb9-a910-e053-dadaa90a0b85e7649bf8-266d-4ef2-aaea-ae12a1f6bcd6

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
55700-726-30EA - Each55700-72665155eba-a9a1-4cf0-bce6-48f1f30f660412019-03-12
55700-726-60EA - Each55700-726259033fb-635f-4177-90ec-385756debc1a12019-03-12
55700-726-90EA - Each55700-72665500013-189b-4687-b401-af79fb737b4112019-03-12