Aurobindo Pharma Share Price Target at Rs 1,430: Motilal Oswal Research

Aurobindo Pharma Share Price Target at Rs 1,430: Motilal Oswal Research

Motilal Oswal Financial Services has issued a Buy recommendation for Aurobindo Pharma Ltd. (ARBP), pegging the current market price at Rs1,208 with a target price of Rs1,430, implying an 18% upside. This assessment, dated 3 December 2025, underscores the company's strategic pivot toward self-sufficiency in critical APIs amid India's push against Chinese import dominance, bolstered by PLI scheme incentives and impending minimum import prices (MIP). Key catalysts include ramped-up Pen-G and 6-APA production, CuraTeQ's biosimilars pipeline targeting a $50 billion market, robust European expansion to EUR1 billion revenue by FY26, and a lucrative biologics CMO pact with Merck Sharp & Dohme (MSD). Analysts project a 9-14-21% CAGR in sales, EBITDA, and PAT over FY26-28, driven by 90 basis points margin expansion and deleveraging, valuing the stock at 16x 12-month forward earnings. Aurobindo stands as India's sole large-scale Pen-G producer, fortifying its moat in generics leadership.

Financial Snapshot (INR b, YE March) FY26E FY27E FY28E
Sales 328.7 368.5 410.4
EBITDA 70.0 80.7 91.1
Adj. PAT 36.3 45.5 53.0
EPS (INR) 62.4 78.3 91.2
RoE (%) 10.6 11.9 12.4
PE (x) 19.3 15.4 13.2

Pen-G6-APA Fortress: Policy Tailwinds Ignite Scale-Up

India's pharmaceutical ecosystem grapples with a stark vulnerability: 70% of API imports, worth $10-12 billion annually, hail from China, fueling calls for strategic indigenization. The government's PLI scheme, launched in 2020, channels incentives toward bulk drugs like Pen-G and 6-APA, pivotal for beta-lactam antibiotics. Aurobindo, having sunk Rs35 billion into its Kakinada complex—Rs27 billion for Pen-G (15,000MT capacity) and Rs8 billion for 6-APA/amoxicillin—commenced commercial Pen-G output in July 2025 post-regulatory nods.

At 40-50% utilization in 2QFY26, annualized production hit 6,000MT, with swift ramp-up to 15,000MT feasible sans demand constraints. Notably, 60% captive consumption slashes costs, conferring a backward integration edge while insulating against geopolitical flux. Imminent MIP notifications for Pen-G, 6-APA, and amoxicillin—mirroring existing curbs on ATS-8 and sulphadiazine—promise pricing parity, expediting breakeven via fuller fixed-cost absorption. Exhibit data reveals India's FY25 Pen-G imports from China at 8,142MT ($853 million) and 6-APA at 10,515MT ($1.5 billion), underscoring Aurobindo's first-mover primacy.

Biosimilars Pipeline: CuraTeQ's Oncology Onslaught

CuraTeQ, Aurobindo's wholly-owned arm, architects a biosimilars odyssey in immunology and oncology, leveraging a 140,000 sq. ft. EU-GMP certified Hyderabad hub with microbial/mammalian bioreactors (up to 2,500L) and end-to-end fill-finish prowess. A 33,000 sq. ft. R&D enclave, manned by 125 scientists, fuels analytical/process/formulation rigor. Four EU-approved products notched first European invoicing in 2QFY26, heralding commercialization.

The late-stage arsenal dazzles: Denosumab (BP16, $5.7 billion osteoporosis market, Phase 3 success, EMA 1QFY27), Omalizumab (BP11, $4 billion urticaria, recruitment done), Tocilizumab (BP08, $3.5 billion RA, Phase 3 waiver), Bevacizumab (BP01, $6.2 billion NSCLC, UK MHRA-approved). Eight more candidates eye $50 billion TAM by 2030, with Phase 3 waivers slashing $50-150 million costs per asset. This positions FY27-28 as a monetization inflection, diversifying beyond generics.

Biosimilar Reference Market (USDb) Status EU/US Launch
Denosumab BP16 Xgeva/Prolia 5.7 Phase 3 Success 1Q/2Q FY27
Omalizumab BP11 Xolair 4 Phase 3 Complete 1Q/3Q FY27
Tocilizumab BP08 Actemra 3.5 Phase 3 Waiver 1Q FY27
Bevacizumab BP01 Avastin 6.2 MHRA Approved 1Q/4Q FY27

European Ascendancy: From 550 INNs to EUR1 Billion

Aurobindo's European foray spans 10 nations, commercializing 550+ INNs across 80% market coverage, aspiring to 85-90%. Constant-currency revenue surged 23% from 2QFY24 to 2QFY26 (EUR243 million), with share ballooning 530 basis points to 29.8% in 1HFY26. A 6,314-filing pipeline, biosimilar infusions, and China OSD ramp (2 billion units, 13 approvals, EBITDA breakeven 3Q-4QFY26) propel FY26 EUR1 billion ambition.

Inorganic bolt-ons, like FY25's Rs180 million Ace Laboratories acquisition for QC analytics, signal portfolio bulking. Management pipelines more M&As, synergizing with organic levers for sustained double-digit expansion.

MSD CMO Pact: Biologics Bonanza Unfolds

TheraNym's FY25 MSA with MSD inaugurates biologics CMO, targeting a $30-40 billion market (9% CAGR to CY30). Initial mammalian cell-culture orders underpin a 15kL bioreactor facility with fill-finish; Block 2 adds two more lines (Rs3.5-4 billion capex). This high-margin vertical complements formulations (9% CAGR FY25-28), offsetting US generics pricing pressures.

Financial Fortitude and Investor Roadmap

Projections paint robust trajectory: US sales 7% CAGR, EU/ROW 14%; EBITDA margins steady 20-22%; EPS CAGR 16% to Rs91.2 (FY28). Net debt-to-equity shrinks to -0.2x, RoE climbs to 12.4%. Lannett integration and injectables pipeline amplify 9/14/21% sales/EBITDA/PAT CAGRs FY26-28.

Key Levels for Traders: Support at Rs1,100 (52-week low proximity), pivot Rs1,208 (CMP), resistance Rs1,365 (52-week high), breakout to Rs1,430 (TP). Investors: Accumulate on dips below Rs1,150 for 18% upside; trail stops at Rs1,100. Highest US generics heft among peers, ANDA trove, and growth vectors—Pen-G scale, biosimilars, EU, CMO—cement BUY reiterated.

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