55700-239 : Cyclobenzaprine Hydrochloride 7.5 mg Oral Tablet, Film Coated

NDC:	55700-239
Labeler:	Lake Erie Medical Dba Quality Care Products LLC
Product Type:	Human Prescription Drug
Drug Name:	Cyclobenzaprine Hydrochloride
Dosage Form:	Oral Tablet, Film Coated
Application #:	ANDA078722
Rev. Date:	Mar 25, 2015

Appearance:

Markings:	RE;33
Shapes:	Round
Colors:	White
Size (mm):	7
Segments: ^*	1
^* Segments = the number of equally sized pieces which the pill can be broken into. In this case, a value of 1 indicates a solid pill with no score lines.

NDC Package Codes:

55700-239-01: 120 TABLET, FILM COATED IN 1 BOTTLE (55700‑239‑01)
55700-239-10: 10 TABLET, FILM COATED IN 1 BOTTLE (55700‑239‑10)
55700-239-30: 30 TABLET, FILM COATED IN 1 BOTTLE (55700‑239‑30)
55700-239-60: 60 TABLET, FILM COATED IN 1 BOTTLE (55700‑239‑60)
55700-239-90: 90 TABLET, FILM COATED IN 1 BOTTLE (55700‑239‑90)

Active Ingredients:

Cyclobenzaprine Hydrochloride

Dosage Strength:

7.5 mg

Inactive Ingredients:

Starch, Corn
Hydroxypropyl Cellulose (Type H)
Hypromelloses
Lactose Monohydrate
Magnesium Stearate
Polyethylene Glycols
Talc
Titanium Dioxide

Pharmaceutical Classes:

Centrally-mediated Muscle Relaxation [PE]
Muscle Relaxant [EPC]

NDC QR Code

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NDC 55700-239 QR Code

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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.