Pregabalin CAS 148553-50-8 For Antiepileptic Treatment
Pregabalin Basic Info
| Product Name |
Pregabalin |
| Alias |
LYRICA |
| CAS |
148553-50-8 |
| MF |
C8H17NO2 |
| MW |
159.23 |
| EINECS |
200-659-6 |
| Purity |
99.50% |
| Grade |
Pharmaceutical Grade |
| Appearance |
White Crystal Powder |
| Brand Nmae |
HKYC |
| Standard |
USP |
| Stock |
Mass Stock |
| Packing Methods |
designed disguised packing ways, 100% pass custom guarantee |
| Delivery time |
within 18 hours after payment confirmed |
| Payment |
T/T, Western Union,Money Gram , Bitcoin |
| Usage |
New antiepileptic drugs. Used in the treatment of peripheral neuropathy, or partial seizures |
How should this medicine be used?
Pregabalin comes as a capsule, an oral solution, and as an extended-release tablet to take by mouth. Pregabalin capsules and oral solution are usually taken with or without food two or three times a day. Pregabalin extended-release tablets are usually taken once daily after an evening meal. Take pregabalin at around the same time(s) every day. Follow the directions on your prescription label carefully, and ask your doctor or pharmacist to explain any part you do not understand.
Swallow the extended-release tablets whole; do not cut, chew, or crush them.
Your doctor will probably start you on a low dose of pregabalin and may gradually increase your dose during the first week of treatment.
Take pregabalin exactly as directed. Pregabalin may be habit forming. Do not take a larger dose, take it more often, or take it for a longer period of time than prescribed by your doctor.
Pregabalin may help control your symptoms but will not cure your condition. It may take several weeks or longer before you feel the full benefit of pregabalin. Continue to take pregabalin even if you feel well. Do not stop taking pregabalin without talking to your doctor, even if you experience side effects such as unusual changes in behavior or mood. If you suddenly stop taking pregabalin, you may experience withdrawal symptoms, including trouble falling asleep or staying asleep, nausea, diarrhea, headaches, or seizures. Your doctor will probably decrease your dose gradually over at least 1 week.
COA:
| ITEMS |
STANDARDS |
RESULTS |
| Appearance |
A white to off white powder |
White powder |
| Identification |
A. Meets the requirement |
Complies |
| B. IR: similar to Reference Substance |
Complies |
| Loss on drying |
≤0.5% |
0.21% |
| Specific Rotation |
+10.0°~+13.0° |
+10.8° |
| Related Substances |
Any single impurity ≤0.1%
Total impurity ≤0.8% |
0.05%
0.10% |
| Purity By HPLC R-isomer |
≤0.15% |
0.10 |
| Residue on ignition |
≤0.1% |
0.05% |
| Residual solvents |
Isopropyl alcohol ≤5000ppm
Ethyl Acetate ≤5000ppm |
150ppm
250ppm |
| Heavy metals |
≤10ppm |
Complies |
| Chlorides |
≤0.05% |
Complies |
| Assay |
98%~102.0% |
99.8% |
| Conclusion |
Analyse according to Factory Standard , Conform |
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