Contact
Naprod Life Sciences Pvt. Ltd. manufactures at a single site: MIDC Tarapur, Boisar, Maharashtra, India (DUNS 915076185). Corporate correspondence starts at the Mumbai head office; choose an enquiry category below and it reaches the team that handles it.
200+ products · 15+ international accreditations · one manufacturing address since 1994.
One corporate point of contact
Head office
Every enquiry sent to the head office is read and routed to a named owner within the company. We value each one, whether it concerns a dossier, a partnership, a role, or a report.
304 Town Center 1, Andheri–Kurla Road, Andheri East
(opposite Times Square Building)
Mumbai 400059, Maharashtra, India
Manufacturing site
Plot No. G17/1, MIDC, Tarapur, Boisar
District Palghar 401506, Maharashtra, India
D-U-N-S® Number 915076185
EU-GMP · ANVISA (Brazil) · INVIMA (Colombia) · UAE MOHAP · NHRA Bahrain · WHO-GMP
Group company
MacChem, a Naprod group company, manufactures the active pharmaceutical ingredients behind Naprod's finished doses. It can be reached directly at the addresses below.
Corporate office
304 Town Centre, 3rd Floor, Andheri–Kurla Road, Andheri (East)
Mumbai 400059, Maharashtra, India
Manufacturing site
N-211/2/10, Tarapur MIDC, Boisar
District Palghar 401506, Maharashtra, India
General enquiries
The form asks for enquiry type, full name, email address, and message, plus optional company and country details. Product complaints and adverse-event reports are not accepted through this form; use the pharmacovigilance path instead.
Naprod handles four recurring enquiry types: (1) export and regulatory, covering dossier status, CoA requests, and market registration support for FDF or API products; (2) CDMO and partnership, covering process development and manufacturing-scale enquiries; (3) product complaints and adverse-event reports, which go through the dedicated pharmacovigilance path below, never through the general enquiry form; and (4) careers, with current openings listed on the Careers page. Selecting a category on the form sends your enquiry directly to the team that handles it.
Product complaints & adverse events
Report a suspected product quality complaint or an adverse event linked to a Naprod-manufactured product through this dedicated path, not the general enquiry form. This channel is for regulated reporting only: batch-specific quality deviations, packaging or labeling defects, and adverse-event observations tied to a specific product and batch number. Reports are logged against the Tarapur facility's quality management system, the same system underlying its EU-GMP, ANVISA, INVIMA, UAE Ministry of Health, NHRA Bahrain, and WHO-GMP accreditations.
Pending approval The pharmacovigilance intake address/phone and the internal SLA for acknowledgment are pending confirmation from the company; this section is a placeholder path, visibly labeled, until the company supplies a live reporting channel. This site makes no medical or therapeutic-benefit claims: this path exists for quality and safety reporting only, not clinical advice.
Verify before you act
Treat any unexpected approach made in Naprod's name with care, whether it arrives by email, phone, messaging app, or social media. This includes recruitment or job offers, requests for money or payment details, fundraising or investment solicitations, and business collaboration proposals claiming to come from Naprod or its representatives.
Genuine correspondence from Naprod comes only from an @naprodgroup.com address. Naprod never asks candidates for money, equipment purchases, training fees, or refundable security deposits at any stage of recruitment; recruitment-specific guidance is published on the Careers page.
To verify any communication claiming to be from Naprod, write to info@naprodgroup.com with the details before responding, making any payment, or sharing personal or financial information.
