Levofloxacin, USP (Hemihydrate)
Levofloxacin USP can be a light yellowish-white to yellow-white crystals or crystalline powder. Alternative name(s): levofloxacin hemihydrate, levofloxacin hydrate
Levofloxacin USP can be a light yellowish-white to yellow-white crystals or crystalline powder. Alternative name(s): levofloxacin hemihydrate, levofloxacin hydrate
Levetiracetam USP is a white to almost white powder.
Levamisole Hydrochloride, USP is a white or almost white powder.
Leuprolide Acetate USP is a white or almost white, hygroscopic powder. Alternative name(s): leuprorelin acetate
Leucovorin Calcium, USP is an odorless, hygroscopic powder that ranges from yellowish-white to yellow in color. Premium Supplement Grade refers to a nutritional supplement that is manufactured by an FDA-registered drug manufacturer. Qualified manufacturers adhere to FDA registration and comply with general facility and equipment-specific GMP standards (21 CFR Parts 210 and 211). Compliance with stability and testing may vary. The customer is responsible for ensuring suitability of the product for the intended use and acknowledges that further testing may be required. Alternative name(s): Calcium folinate, Folinic acid calcium salt
Leucine (L), USP come as white crystals, with a characteristic odor. Validation of grade in progress. Alternative name(s): L-Leucine
Lansoprazole USP is a white to brownish-white hygroscopic powder.
Lactose NF is an odorless, crystalline powder that is white or almost white. Alternative name(s): Lactose Monohydrate
Lactose NF is an odorless, crystalline powder that is white or almost white. Alternative name(s): Lactose Monohydrate
Lactose NF is a white or almost white powder.
Lactic Acid, USP (Racemic) is a colorless or yellowish, practically odorless, syrupy liquid that is miscible with both water and with alcohol. It is hygroscopic. Dietary Supplement Grade refers to a nutritional supplement that is manufactured by an FDA-registered dietary supplement manufacturer or manufacturer with other certifications and registrations, based on applicable laws and regulations. Qualified manufacturers follow their applicable standards of practice, which are less stringent than those for FDA-registered drug manufacturers. The customer is responsible for ensuring suitability of the product for the intended use and acknowledges that further testing may be required.