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API Name : Limonene
- Labelled stable isotope standards-API'S & API Impurities
- Labetalol
- Lacidipine
- Lacosamide
- Lactitol
- Lactobionic Acid
- Lactofen
- Lactoferrin
- Lactose
- Lactulose
- Lafutidine
- Laidlomycin
- Lamivudine
- Lamotrigine
- Landiolol
- Laninamivir
- Lanreotide
- Lansoprazole
- Lapatinib
- Larotrectinib
- Lasiocarpine
- Lasmiditan
- Latanoprost
- Lecirelin
- Ledipasvir
- Leflunomide
- Lemborexant
- Leminoprazole
- Lenacapavir
- Lenalidomide
- leniolisib
- Lenvatinib
- Lercanidipine
- Lesinurad
- Letermovir
- Letrozole
- Leucine
- leucovorin
- Leuprolide
- Levalbuterol
- Levamisole
- Levetiracetam
- Levobunolol
- Levocabastine Hydrochloride
- Levocarnitine
- Levocetirizine
- Levocloperastine Fendizoate
- Levodopa
- Levodropropizine
- Levofloxacin
- Levofolinate
- Levomefolate
- Levomepromazine
- Levomilnacipran
- Levonorgestrel
- Levorphanol
- Levosimendan
- Levosulpiride
- Levothyroxine
- Lidocaine
- Lifitegrast
- Limaprost
- Limonene
- Linaclotide
- Linagliptin
- Linaprazan
- Lincomycin Hydrochloride
- Linezolid
- Linolenic Acid
- Liothyronine
- Lipoic acid
- Liraglutide
- Lisaftoclax
- Lisdexamfetamine
- Lisinopril
- Litoxetine
- Lobeglitazone
- Lofepramine
- Lofexidine
- Lomefloxacin
- Lomitapide
- Lomustine
- Lonafarnib
- Lopamidol
- Loperamide
- Lopinavir
- Loprazolam
- Loratadine
- Lorazepam
- Lorcaserin
- Lorlatinib
- Lornoxicam
- Losartan
- Loteprednol
- Lotilaner
- Lovastatin
- Loxapine
- Loxoprofen
- Lubiprostone
- Lufenuron
- Luliconazole
- Lumacaftor
- Lumateperone
- Lumefantrine
- Lupeol
- Lurasidone
- Lusutrombopag
- Luteolin
- Lycopsamine
- Lycorine
- Lymecycline
- Lynestrenol
- Lypressin
- Lysergide
- Lysergol
- Lysine
Limonene
Venkatasai is a leading provider of pharmaceutical reference standards, specializing in the supply of high-purity Limonene reference materials. Our portfolio includes both pharmacopeial and non-pharmacopeial impurities, metabolites, stable isotope-labeled compounds, and nitrosamine derivatives (N-NO products). These reference standards play a crucial role in pharmaceutical R&D, aiding in formulation development, ANDA/DMF submissions, quality control, method validation, stability studies, and impurity profiling—including the identification and assessment of potentially genotoxic impurities.
Each Limonene-related product is rigorously characterized and delivered with a detailed Certificate of Analysis (COA) and comprehensive analytical data to ensure regulatory compliance. Upon request, we also offer EP/USP traceable standards. To maintain the highest quality standards, all materials are subject to periodic re-testing and continuous quality monitoring.
