Tamsulosin Hydrochloride Modified Release 0.4 mg Tablets — Tablets
WHO-GMP Certified Commercial Pack · Product Code: AKP-353

Tamsulosin Hydrochloride Modified Release 0.4 mg Tablets

Formulation Overview: 24-hour modified-release uroselective alpha-1A/1D blocker tablet engineered for flat plasma pharmacokinetics, steady urinary relief, and low dizziness incidence. Formulated with Tamsulosin Hydrochloride MR 0.4 mg (0.4 mg (Modified Release)) in Modified-Release Tablets dosage form under Sexual Wellness Medication, manufactured to IP / BP / USP Compendial standards and supplied in 10 x 10 Alu-Alu / Blister Pack with complete eCTD/ACTD regulatory dossiers, Zone IVb stability, and batch CoA for African NRAs (NAFDAC, PPB, SAHPRA, TMDA, FDA Ghana) and global tenders.
Item Code (SKU)AKP-353
Catalog ReferenceAKP-353 · SN 353
Therapeutic SectorSexual Wellness Medication
Dosage FormModified-Release Tablets
Active IngredientTamsulosin Hydrochloride MR 0.4 mg
Strength / Purity0.4 mg (Modified Release)
Clinical IndicationFunctional symptoms of benign prostatic hyperplasia (BPH) and impaired urinary flow
Specification StandardIP / BP / USP Compendial
Packaging Format10 x 10 Alu-Alu / Blister Pack
Shelf Life24–36 Months
Storage ConditionsStore below 25°C in a dry place, protect from light and moisture
Minimum Order Quantity1000 Packs
Regulatory / Analytical DocsFull eCTD / ACTD Modules 1–5 + Zone IVb Stability Available
African & Global NRA ReadinessNAFDAC (Nigeria), PPB (Kenya), SAHPRA (SA), TMDA (Tanzania), FDA Ghana, AIRP, ARP, EFDA
Stock AvailabilityIn Stock · Immediate Commercial Dispatch
Supply StatusCommercial Export Ready

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