White Round Pill With D On One Side And 31 The Other What Is It (Top voted first)

I received this pill for a generic form of soma.It is making me feel like a tylenol 3mg would which is something I can't take.Do you have information on this? The brand I was on is manufatured by watson..this is manufatured by sun pharmaceuti.What am I taking?

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The round white pill you are describing with an imprint of D 31 is identified as Carisoprodol (350 mg). I wasn't able to verify the manufacturer however, but the national drug code (NDC) for this pill is: 65862-0158

Carisoprodol is a centrally-acting skeletal muscle relaxant.

To learn more information about this drug, please refer to the link below...
https:/­/­rxchat.com/­wiki/­Carisoprodol/­

I hope this helps!

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Yes, it is Carisoprodol, which is generic for Soma. I got the same one, after always being given the generic manufactured by Watson labs. The label on this prescription (for the one with the "D" on one side and "31" on the other) says it is manufactured by Aurobindo Pharmaceuticals. I never even heard of this lab, so it must be a new one. Or at least new to manufacturing generic Soma.

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After reading this about Aurobindo I'm not sure I'd trust this Indian company?

The U.S. Food and Drug Administration (FDA) conducted inspections of Aurobindo Pharma Limited, Unit III (hereinafter referred to as "Unit III"), located at Survey Nos. 313/314, Bachupally, Quthubullapur Mandal, Hyderabad, Andhra Pradesh, India, and Aurobindo Pharma Limited, Unit VI (hereinafter referred to as "Unit VI"), located at Survey Nos. 329/39 & 329/47, Chitkul Village, Patancheru Mandal, Medak Dist, Andhra Pradesh, 502 307, India. The inspection of Unit III took place during September 20 - 24, 2010 (September 2010 inspection). The inspection of Unit VI took place during December 7 - 22, 2010 (December 2010 inspection).

During our inspection of Unit VI, and through Field Alert Reports related to Unit III, FDA identified significant violations of Current Good Manufacturing Practice (CGMP) regulations for Finished Pharmaceuticals, Title 21, Code of Federal Regulations, Parts 210 and 211. In addition, violations of section 501(a)(2)(B) of the Federal Food, Drug, and Cosmetic Act (the Act) [21 U.S.C. § 351(a)(2)(B)] were documented with respect to APIs. These violations cause your drugs to be adulterated within the meaning of section 501(a)(2)(B) of the Act in that the methods used in, or the facilities or controls used for, their manufacture, processing, packing, or holding do not conform to, or are not operated or administered in conformity with, CGMP.

Unit VI

We have reviewed your January 13, 2011 response to the Form FDA-483 issued at the conclusion of the December 2010 Unit VI inspection, and note that it lacks sufficient corrective actions.

Specific violations observed during the inspection include, but are not limited, to the following:
Your firm’s laboratory records fail to include complete data derived from all tests necessary to assure compliance with established specifications and standards [21 C.F.R. § 211.194].
For example,
On December 13, 2010, the FDA investigator observed a microbiological plate that contained one (1) large colony forming unit (CFU) of mold. However, your firm’s laboratory documentation reported 0 CFU for the same microbiological plate

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You must do a Search on Aurobindo from India. The FDA Found their facilities full of filth, not like that can't happen here?

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