50090-3211 : Carisoprodol 350 mg Oral Tablet

NDC:	50090-3211
Labeler:	A-s Medication Solutions
Product Type:	Human Prescription Drug
Drug Name:	Carisoprodol
Dosage Form:	Oral Tablet
Application #:	ANDA205085
Rev. Date:	Jun 1, 2015
CSA Schedule:	CIV (US) ^[1]

^[1] Schedule IV Controlled Substance: Low potential for abuse relative to substances in Schedule III. Examples include Alprazolam (Xanax), Diazepam (Valium), Carisoprodol (Soma), Clonazepam (Klonopin), Lorazepam (Ativan), Clorazepate (Tranxene), Midazolam (Versed), Temazepam (Restoril), and Triazolam (Halcion).. More Details: US Dept of Justice Controlled Substance Schedules.

Appearance:

Markings:	OP;35
Shapes:	Round
Colors:	White
Size (mm):	12
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:

50090-3211-0: 30 TABLET IN 1 BOTTLE (50090‑3211‑0)
50090-3211-3: 20 TABLET IN 1 BOTTLE (50090‑3211‑3)
50090-3211-8: 60 TABLET IN 1 BOTTLE (50090‑3211‑8)
50090-3211-9: 120 TABLET IN 1 BOTTLE (50090‑3211‑9)

Active Ingredients:

Carisoprodol

Dosage Strength:

350 mg

Inactive Ingredients:

Lactose Monohydrate
Microcrystalline Cellulose
Magnesium Stearate
Croscarmellose Sodium
Povidone K30
Talc
Starch, Corn /

Pharmaceutical Classes:

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

NDC 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.