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.
